Resource

Id	TF_ChIP-seq/ENCSR000BSAcontent_copy
Type	position_score
Version	0
Summary	TF_ChIP-seq ENCSR000BSA [biosample_summary="Homo sapiens HCT116" and target="JUND"]
Description
Labels	accession: ENCSR000BSA assay_term_name: ChIP-seq biosample_ontology: /biosample-types/cell_line_EFO_0002824/ biosample_summary: Homo sapiens HCT116 date_created: 2013-12-19T20:51:44.392677+00:00 date_released: 2012-09-10 doi: 10.17989/ENCSR000BSA perturbed: False reference_genome: hg38/genomes/GRCh38-hg38 replication_type: isogenic simple_biosample_summary: status: released submitter_comment: target: JUND

Scores (1)

ID	Type	Default annotation	Description	Histogram	Range	Summary
TF_ChIP-seq_ENCSR000BSA	float	TF_ChIP-seq_ENCSR000BSA	TF_ChIP-seq ENCSR000BSA [biosample_summary="Homo sapiens HCT116" and target="JUND"]		[5.42, 455]	n 8,418,287 mean 56.7 sd 49.9

n counts base pairs; sd is the population standard deviation.

Chromosome	Covered positions	Covered %	Segments
all chromosomes	8418287	0.26%	25874
chr1	844723	0.34%	2605
chr1_KI270713v1_random	1275	3.13%	6
chr2	725963	0.30%	2205
chr3	609488	0.31%	1898
chr4	527448	0.28%	1604
chr5	449167	0.25%	1356
chr6	637432	0.37%	1991
chr7	445107	0.28%	1370
chr8	443735	0.31%	1414
chr9	305747	0.22%	952
chr10	474162	0.35%	1480
chr11	375117	0.28%	1124
chr12	506993	0.38%	1574
chr13	157234	0.14%	460
chr14	219014	0.20%	676
chr15	215694	0.21%	662
chr16	216677	0.24%	650
chr17	358093	0.43%	1114
chr18	162695	0.20%	478
chr19	196864	0.34%	635
chr20	198237	0.31%	596
chr21	49207	0.11%	145
chr22	111938	0.22%	327
chrM	7384	44.57%	31
chrUn_KI270466v1	396	32.12%	1
chrX	178497	0.11%	520
3340 contigs with no values (186245953 bp)	0	0.00%	0

	segments	min	max	mean	median
segments	25874	1	746	325.36	396