Resource

Id	TF_ChIP-seq/ENCSR000BGUcontent_copy
Type	position_score
Version	0
Summary	TF_ChIP-seq ENCSR000BGU [biosample_summary="Homo sapiens GM12878" and target="EBF1"]
Description
Labels	accession: ENCSR000BGU assay_term_name: ChIP-seq biosample_ontology: /biosample-types/cell_line_EFO_0002784/ biosample_summary: Homo sapiens GM12878 date_created: 2013-09-13T15:58:25.880581-08:00 date_released: 2011-07-18 doi: 10.17989/ENCSR000BGU perturbed: False reference_genome: hg38/genomes/GRCh38-hg38 replication_type: isogenic simple_biosample_summary: status: released submitter_comment: target: EBF1

Scores (1)

ID	Type	Default annotation	Description	Histogram	Range	Summary
TF_ChIP-seq_ENCSR000BGU	float	TF_ChIP-seq_ENCSR000BGU	TF_ChIP-seq ENCSR000BGU [biosample_summary="Homo sapiens GM12878" and target="EBF1"]		[4.45, 511]	n 10,072,814 mean 62.7 sd 69

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

Chromosome	Covered positions	Covered %	Segments
all chromosomes	10072814	0.31%	42710
chr1	970532	0.39%	4092
chr2	747001	0.31%	3191
chr3	615113	0.31%	2602
chr4	353694	0.19%	1497
chr5	544686	0.30%	2282
chr6	597664	0.35%	2553
chr7	464270	0.29%	1952
chr8	419713	0.29%	1771
chr9	414363	0.30%	1766
chr10	492692	0.37%	2077
chr11	510126	0.38%	2178
chr12	468039	0.35%	1988
chr13	210210	0.18%	894
chr14	362628	0.34%	1545
chr15	362938	0.36%	1546
chr16	426053	0.47%	1799
chr17	538773	0.65%	2290
chr18	203000	0.25%	866
chr19	463715	0.79%	1965
chr20	300941	0.47%	1263
chr21	123248	0.26%	523
chr22	264501	0.52%	1125
chrX	218914	0.14%	945
3343 contigs with no values (186304500 bp)	0	0.00%	0

	segments	min	max	mean	median
segments	42710	1	895	235.84	264