Variant report

Variant	rs28362586
Chromosome Location	chr4:2795474-2795475
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MAZ	chr4:2795378-2795888	GM12878	blood:	n/a	n/a
2	POLR2A	chr4:2795260-2795696	MCF10A-Er-Src	breast:	n/a	n/a
3	JUND	chr4:2795353-2796034	K562	blood:	n/a	n/a
4	POLR2A	chr4:2795465-2796130	HepG2	liver:	n/a	n/a
5	HMGN3	chr4:2795327-2795611	K562	blood:	n/a	n/a
6	STAT3	chr4:2795252-2795609	MCF10A-Er-Src	breast:	n/a	chr4:2795392-2795412 chr4:2795392-2795412 chr4:2795390-2795402 chr4:2795397-2795406 chr4:2795398-2795407 chr4:2795398-2795406 chr4:2795396-2795407
7	MAX	chr4:2795255-2796216	K562	blood:	n/a	chr4:2795869-2795879
8	SMARCB1	chr4:2794940-2796147	Hela-S3	cervix:	n/a	n/a
9	JUND	chr4:2795452-2795623	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:2795327-2795641	H1-hESC	embryonic stem cell:	n/a	n/a
11	HA-E2F1	chr4:2795297-2796155	MCF-7	breast:	n/a	chr4:2795620-2795627 chr4:2795566-2795578 chr4:2795620-2795627 chr4:2795620-2795627 chr4:2795566-2795575
12	E2F4	chr4:2795318-2795609	MCF10A-Er-Src	breast:	n/a	chr4:2795566-2795578 chr4:2795566-2795575
13	MYC	chr4:2795469-2796608	MCF10A-Er-Src	breast:	n/a	chr4:2795869-2795879
14	MAZ	chr4:2795172-2797101	IMR90	lung:	n/a	chr4:2796846-2796857
15	MAX	chr4:2795344-2796804	A549	lung:	n/a	chr4:2795869-2795879
16	POLR2A	chr4:2795315-2795596	Hela-S3	cervix:	n/a	n/a
17	FOS	chr4:2795387-2795610	MCF10A-Er-Src	breast:	n/a	n/a
18	TFAP2A	chr4:2795374-2796862	Hela-S3	cervix:	n/a	chr4:2796410-2796422 chr4:2796538-2796547 chr4:2795930-2795945
19	POLR2A	chr4:2795332-2795601	Hela-S3	cervix:	n/a	n/a
20	ZMIZ1	chr4:2795424-2795898	K562	blood:	n/a	n/a
21	EP300	chr4:2795359-2797144	SK-N-SH	brain:	n/a	n/a
22	EBF1	chr4:2795321-2795583	GM12878	blood:	n/a	n/a
23	FOS	chr4:2795437-2795541	MCF10A-Er-Src	breast:	n/a	n/a
24	ZNF143	chr4:2795317-2795678	GM12878	blood:	n/a	n/a
25	POLR2A	chr4:2795202-2796999	U87	brain:	n/a	n/a
26	FOSL1	chr4:2795363-2795609	K562	blood:	n/a	chr4:2795466-2795477
27	MAX	chr4:2795346-2797194	HepG2	liver:	n/a	chr4:2795869-2795879 chr4:2796846-2796857
28	TEAD4	chr4:2795291-2795893	K562	blood:	n/a	n/a
29	ZBTB7A	chr4:2794414-2795651	K562	blood:	n/a	n/a
30	MAX	chr4:2795356-2796286	HepG2	liver:	n/a	chr4:2795869-2795879
31	E2F6	chr4:2795313-2796237	K562	blood:	n/a	chr4:2795620-2795627 chr4:2795566-2795578 chr4:2795620-2795627 chr4:2795620-2795627 chr4:2795566-2795575
32	POLR2A	chr4:2795249-2796837	U87	brain:	n/a	n/a
33	STAT3	chr4:2795292-2795870	MCF10A-Er-Src	breast:	n/a	chr4:2795392-2795412 chr4:2795392-2795412 chr4:2795390-2795402 chr4:2795397-2795406 chr4:2795398-2795407 chr4:2795398-2795406 chr4:2795396-2795407
34	SIN3AK20	chr4:2795312-2795558	SK-N-SH	brain:	n/a	n/a
35	SMARCC1	chr4:2795173-2796619	Hela-S3	cervix:	n/a	n/a
36	CCNT2	chr4:2795205-2795945	K562	blood:	n/a	chr4:2795566-2795575
37	TAF1	chr4:2795347-2795601	Hela-S3	cervix:	n/a	n/a
38	FOS	chr4:2795424-2795981	MCF10A-Er-Src	breast:	n/a	n/a
39	JUN	chr4:2795252-2796109	K562	blood:	n/a	chr4:2795899-2795912
40	UBTF	chr4:2795313-2795540	K562	blood:	n/a	n/a
41	ZBTB7A	chr4:2794263-2795708	ECC-1	luminal epithelium:	n/a	n/a
42	POLR2A	chr4:2795180-2796858	HL-60	blood:	n/a	n/a
43	STAT1	chr4:2794835-2796475	Hela-S3	cervix:	n/a	chr4:2795392-2795412 chr4:2795392-2795412 chr4:2795390-2795402 chr4:2795397-2795406 chr4:2795396-2795407 chr4:2795398-2795407 chr4:2795398-2795406
44	ZBTB7A	chr4:2794445-2795639	K562	blood:	n/a	n/a
45	POLR2A	chr4:2795208-2796999	U87	brain:	n/a	n/a
46	POLR2A	chr4:2795333-2795590	K562	blood:	n/a	n/a
47	MAX	chr4:2795191-2797016	A549	lung:	n/a	chr4:2795869-2795879 chr4:2796846-2796857
48	EBF1	chr4:2795470-2795725	GM12878	blood:	n/a	chr4:2795644-2795653
49	RAD21	chr4:2795297-2795745	IMR90	lung:	n/a	n/a
50	RFX5	chr4:2795408-2795529	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:2795439-2795489	NHDF-neo	bronchial:	n/a
2	chr4:2795456-2795506	AG04450	lung:	fetal
3	chr4:2795456-2795506	K562	blood:	n/a
4	chr4:2795439-2795489	HRE	kidney:	n/a
5	chr4:2795456-2795506	HUVEC	blood vessel:	n/a
6	chr4:2795439-2795489	HRCEpiC	kidney:	n/a
7	chr4:2795456-2795506	HEEpiC	esophagus:	n/a
8	chr4:2795456-2795506	CMK	blood:	n/a
9	chr4:2795439-2795489	HNPCEpiC	eye:	n/a
10	chr4:2795456-2795506	NB4	blood:	n/a
11	chr4:2795439-2795489	HIPEpiC	eye:	n/a
12	chr4:2795439-2795489	HMEC	breast:	n/a
13	chr4:2795456-2795506	BE2_C	brain:	n/a
14	chr4:2795439-2795489	HCF	heart:	n/a
15	chr4:2795439-2795489	AG09309	skin:	n/a
16	chr4:2795456-2795506	MCF-7	breast:	n/a
17	chr4:2795439-2795489	HCM	heart:	n/a
18	chr4:2795456-2795506	SK-N-SH	brain:	n/a
19	chr4:2795439-2795489	GM19239	blood:	n/a
20	chr4:2795456-2795506	HL-60	blood:	n/a
21	chr4:2795439-2795489	HRPEpiC	eye:	n/a
22	chr4:2795456-2795506	HepG2	liver:	n/a
23	chr4:2795439-2795489	SK-N-SH	brain:	n/a
24	chr4:2795439-2795489	SAEC	small airway:	n/a
25	chr4:2795456-2795506	NHBE	bronchial:	n/a
26	chr4:2795439-2795489	AoSMC	blood vessel:	n/a
27	chr4:2795439-2795489	ovcar-3	ovarian:	n/a
28	chr4:2795439-2795489	HCPEpiC	choroid plexus:	n/a
29	chr4:2795456-2795506	SKMC	muscle:	n/a
30	chr4:2795456-2795506	HCPEpiC	choroid plexus:	n/a
31	chr4:2795439-2795489	RPTEC	kidney:	n/a
32	chr4:2795439-2795489	Hela-S3	cervix:	n/a
33	chr4:2795439-2795489	GM06990	blood:	n/a
34	chr4:2795456-2795506	NH-A	brain:	n/a
35	chr4:2795456-2795506	T-47D	breast:	n/a
36	chr4:2795439-2795489	HPAEpiC	pulmonary alveolar:	n/a
37	chr4:2795439-2795489	AG04449	skin:	fetal
38	chr4:2795439-2795489	HAEpiC	amniotic membrane:	n/a
39	chr4:2795439-2795489	HL-60	blood:	n/a
40	chr4:2795456-2795506	RPTEC	kidney:	n/a
41	chr4:2795456-2795506	HRE	kidney:	n/a
42	chr4:2795456-2795506	SK-N-MC	brain:	n/a
43	chr4:2795439-2795489	U87	brain:	n/a
44	chr4:2795439-2795489	HEK293	kidney:	embryo
45	chr4:2795456-2795506	MCF10A-Er-Src	breast:	n/a
46	chr4:2795456-2795506	U87	brain:	n/a
47	chr4:2795439-2795489	SK-N-MC	brain:	n/a
48	chr4:2795456-2795506	HCT-116	colon:	n/a
49	chr4:2795439-2795489	Jurkat	blood:	n/a
50	chr4:2795456-2795506	Caco-2	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:2794178..2796870-chr4:2828744..2832985,4	MCF-7	breast:
2	chr4:2794084..2803742-chr4:2816227..2824357,23	MCF-7	breast:
3	chr17:56708745..56710384-chr4:2792772..2795707,2	MCF-7	breast:
4	chr4:2795447..2803617-chr4:2934606..2939244,18	MCF-7	breast:
5	chr4:2790052..2809152-chr4:2930639..2948075,83	MCF-7	breast:
6	chr4:2795244..2797486-chr4:2845439..2847269,2	MCF-7	breast:
7	chr4:2794525..2804465-chr4:2841103..2847851,19	MCF-7	breast:
8	chr4:2793663..2796017-chr4:2810077..2811741,2	MCF-7	breast:
9	chr4:2755902..2759354-chr4:2793552..2797883,6	K562	blood:
10	chr4:2753714..2768807-chr4:2789818..2806638,47	MCF-7	breast:
11	chr4:2757714..2759449-chr4:2793017..2796252,4	K562	blood:
12	chr4:2794820..2799191-chr4:2824314..2827597,4	MCF-7	breast:
13	chr4:2793845..2803067-chr4:2816443..2823671,22	MCF-7	breast:
14	chr4:2747261..2749525-chr4:2793563..2796343,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADD1-6	chr4:2795451-2795484	NONHSAT094808

Variant related genes	Relation type
SH3BP2	TF binding region
SH3BP2	CpG island
ENSG00000168884	Chromatin interaction
ENSG00000249673	Chromatin interaction
ENSG00000109736	Chromatin interaction
ENSG00000087269	Chromatin interaction
ENSG00000087274	Chromatin interaction
ENSG00000087266	Chromatin interaction
ENSG00000212195	Chromatin interaction

Extended variants
information (count: 23 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948659	chr4:1828867-2815632	ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
2	nsv1005116	chr4:2633935-2812340	Bivalent/Poised TSS Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv878444	chr4:2689449-2861090	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv470002	chr4:2701098-2836628	Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv878445	chr4:2704046-2831383	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv878446	chr4:2710644-2810634	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv878447	chr4:2723531-2831383	Flanking Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
8	nsv516797	chr4:2723531-2836628	Strong transcription Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
9	nsv878448	chr4:2723531-2846799	Flanking Active TSS Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
10	esv3418626	chr4:2741174-3461492	Genic enhancers Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
11	esv3397632	chr4:2741239-3460583	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
12	nsv878449	chr4:2744480-2831383	Genic enhancers Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
13	nsv1002517	chr4:2747905-2822017	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
14	nsv878450	chr4:2760222-2861090	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
15	nsv967941	chr4:2765555-2802771	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
16	nsv593435	chr4:2770772-2881256	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
17	nsv878451	chr4:2785556-2856687	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
18	nsv878452	chr4:2789184-2830076	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
19	nsv1010533	chr4:2792848-2873441	Enhancers Bivalent/Poised TSS Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
20	esv3439511	chr4:2793779-2796327	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
21	esv3430511	chr4:2794104-2796177	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
22	nsv461162	chr4:2794320-2846799	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
23	nsv593436	chr4:2794320-2846799	Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:2794200-2795600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr4:2794200-2795600	Active TSS	Small Intestine	intestine
3	chr4:2794400-2795600	Active TSS	H9 Cell Line	embryonic stem cell
4	chr4:2794400-2795600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
5	chr4:2794400-2795600	Enhancers	Fetal Brain Male	brain
6	chr4:2794400-2795600	Active TSS	Fetal Brain Female	brain
7	chr4:2794400-2795800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
8	chr4:2794400-2796000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
9	chr4:2794400-2796000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
10	chr4:2794600-2795600	Active TSS	Primary neutrophils fromperipheralblood	blood
11	chr4:2794600-2795600	Active TSS	Ovary	ovary
12	chr4:2794600-2795600	Active TSS	HepG2	liver
13	chr4:2794800-2795600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
14	chr4:2794800-2795600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr4:2794800-2795600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr4:2794800-2795600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr4:2794800-2795600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr4:2794800-2795600	Active TSS	Breast Myoepithelial Primary Cells	Breast
19	chr4:2794800-2795600	Active TSS	Primary monocytes fromperipheralblood	blood
20	chr4:2794800-2795600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr4:2794800-2795600	Active TSS	Muscle Satellite Cultured Cells	--
22	chr4:2794800-2795600	Active TSS	Brain Anterior Caudate	brain
23	chr4:2794800-2795600	Active TSS	Brain Substantia Nigra	brain
24	chr4:2794800-2795600	Active TSS	Colonic Mucosa	Colon
25	chr4:2794800-2795600	Active TSS	Duodenum Smooth Muscle	Duodenum
26	chr4:2794800-2795600	Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr4:2794800-2795600	Active TSS	Gastric	stomach
28	chr4:2794800-2795600	Active TSS	Sigmoid Colon	Sigmoid Colon
29	chr4:2794800-2795600	Active TSS	Hela-S3	cervix
30	chr4:2794800-2795600	Active TSS	Monocytes-CD14+_RO01746	blood
31	chr4:2794800-2795600	Active TSS	NH-A	brain
32	chr4:2794800-2795600	Active TSS	NHDF-Ad	bronchial
33	chr4:2794800-2795800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr4:2794800-2796000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
35	chr4:2794800-2796000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
36	chr4:2794800-2796200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
37	chr4:2794800-2796400	Flanking Active TSS	Primary B cells from peripheral blood	blood
38	chr4:2794800-2796400	Flanking Active TSS	Primary hematopoietic stem cells	blood
39	chr4:2794800-2796400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr4:2794800-2796400	Flanking Active TSS	Fetal Muscle Leg	muscle
41	chr4:2794800-2796800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr4:2794800-2797200	Flanking Active TSS	Primary B cells from cord blood	blood
43	chr4:2794800-2797200	Flanking Active TSS	Placenta	Placenta
44	chr4:2795000-2795600	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr4:2795000-2795800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
46	chr4:2795000-2795800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr4:2795000-2795800	Flanking Active TSS	HMEC	breast
48	chr4:2795000-2796000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
49	chr4:2795200-2795600	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr4:2795200-2795600	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin

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