Variant report

Variant	rs547200803
Chromosome Location	chr7:4923153-4923154
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	MAX	chr7:4923068-4923651	H1-hESC	embryonic stem cell:	n/a	chr7:4923127-4923137 chr7:4923549-4923559
2	CCNT2	chr7:4922509-4923651	K562	blood:	n/a	chr7:4923466-4923475 chr7:4923590-4923599 chr7:4923551-4923560
3	ETS1	chr7:4923145-4923374	K562	blood:	n/a	n/a
4	POLR2A	chr7:4923124-4923372	ECC-1	luminal epithelium:	n/a	n/a
5	YY1	chr7:4923084-4923590	SK-N-SH_RA	brain:	n/a	chr7:4923379-4923390 chr7:4923312-4923326 chr7:4923282-4923296 chr7:4923126-4923135 chr7:4923551-4923560 chr7:4923242-4923251 chr7:4923548-4923562
6	TAF1	chr7:4923113-4923405	H1-hESC	embryonic stem cell:	n/a	n/a
7	POLR2A	chr7:4923152-4923333	A549	lung:	n/a	n/a
8	E2F6	chr7:4922094-4923618	K562	blood:	n/a	chr7:4923242-4923251 chr7:4922864-4922878 chr7:4923414-4923429 chr7:4923252-4923263 chr7:4923551-4923560 chr7:4923446-4923455
9	POLR2A	chr7:4921914-4923705	H1-neurons	neurons:	n/a	n/a
10	MAX	chr7:4923038-4923603	SK-N-SH	brain:	n/a	chr7:4923127-4923137 chr7:4923549-4923559 chr7:4923057-4923066 chr7:4923061-4923070
11	CTCF	chr7:4923128-4923613	HepG2	liver:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
12	MAX	chr7:4923099-4923620	A549	lung:	n/a	chr7:4923127-4923137 chr7:4923549-4923559
13	RAD21	chr7:4923088-4923681	HepG2	liver:	n/a	chr7:4923439-4923453 chr7:4923544-4923558 chr7:4923318-4923332 chr7:4923504-4923523
14	RAD21	chr7:4923042-4923675	K562	blood:	n/a	chr7:4923439-4923453 chr7:4923544-4923558 chr7:4923318-4923332 chr7:4923504-4923523
15	CTCF	chr7:4923107-4923710	K562	blood:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
16	ZBTB7A	chr7:4922593-4923485	ECC-1	luminal epithelium:	n/a	chr7:4923170-4923177
17	CTCF	chr7:4923092-4923733	K562	blood:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
18	CTCF	chr7:4923077-4923658	H1-hESC	embryonic stem cell:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
19	CTCF	chr7:4923121-4923914	HCT-116	colon:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923748-4923761 chr7:4923319-4923332 chr7:4923314-4923332
20	MAX	chr7:4922990-4923751	MCF-7	breast:	n/a	chr7:4923127-4923137 chr7:4923549-4923559 chr7:4923057-4923066 chr7:4923061-4923070
21	POLR2A	chr7:4923009-4923387	PFSK-1	brain:	n/a	n/a
22	CREB1	chr7:4923021-4923782	HepG2	liver:	n/a	n/a
23	CTCF	chr7:4923122-4923741	MCF-7	breast:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
24	MAX	chr7:4922982-4923531	ECC-1	luminal epithelium:	n/a	chr7:4923127-4923137 chr7:4923057-4923066 chr7:4923061-4923070
25	YY1	chr7:4923093-4923623	SK-N-SH_RA	brain:	n/a	chr7:4923379-4923390 chr7:4923312-4923326 chr7:4923282-4923296 chr7:4923126-4923135 chr7:4923551-4923560 chr7:4923242-4923251 chr7:4923548-4923562
26	POLR2A	chr7:4923145-4923359	H1-hESC	embryonic stem cell:	n/a	n/a
27	MAX	chr7:4922976-4923694	HepG2	liver:	n/a	chr7:4923127-4923137 chr7:4923549-4923559 chr7:4923057-4923066 chr7:4923061-4923070
28	YY1	chr7:4923096-4923576	K562	blood:	n/a	chr7:4923379-4923390 chr7:4923312-4923326 chr7:4923282-4923296 chr7:4923126-4923135 chr7:4923551-4923560 chr7:4923242-4923251 chr7:4923548-4923562
29	MAX	chr7:4922997-4923678	H1-hESC	embryonic stem cell:	n/a	chr7:4923127-4923137 chr7:4923549-4923559 chr7:4923057-4923066 chr7:4923061-4923070
30	POLR2A	chr7:4923039-4923477	K562	blood:	n/a	n/a
31	MXI1	chr7:4921317-4924106	SK-N-SH	brain:	n/a	chr7:4923055-4923070
32	CTCF	chr7:4922936-4923720	K562	blood:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923020-4923030 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332
33	RAD21	chr7:4923085-4923760	MCF-7	breast:	n/a	chr7:4923439-4923453 chr7:4923544-4923558 chr7:4923318-4923332 chr7:4923504-4923523
34	EGR1	chr7:4923140-4923887	K562	blood:	n/a	chr7:4923765-4923778 chr7:4923545-4923560 chr7:4923551-4923561 chr7:4923764-4923779 chr7:4923379-4923392 chr7:4923546-4923559 chr7:4923766-4923777
35	POLR2A	chr7:4923044-4923451	Gliobla	brain:	n/a	n/a
36	POLR2A	chr7:4922980-4923517	H1-neurons	neurons:	n/a	n/a
37	E2F6	chr7:4923099-4923726	H1-hESC	embryonic stem cell:	n/a	chr7:4923242-4923251 chr7:4923414-4923429 chr7:4923252-4923263 chr7:4923551-4923560 chr7:4923446-4923455
38	MAX	chr7:4923092-4923662	K562	blood:	n/a	chr7:4923127-4923137 chr7:4923549-4923559
39	RFX5	chr7:4923008-4923580	HepG2	liver:	n/a	chr7:4923056-4923071 chr7:4923056-4923071 chr7:4923061-4923070 chr7:4923058-4923073 chr7:4923059-4923073 chr7:4923056-4923071 chr7:4923058-4923071 chr7:4923055-4923072
40	RAD21	chr7:4923101-4923744	ECC-1	luminal epithelium:	n/a	chr7:4923439-4923453 chr7:4923544-4923558 chr7:4923318-4923332 chr7:4923504-4923523
41	BHLHE40	chr7:4922963-4923635	K562	blood:	n/a	chr7:4923312-4923328 chr7:4923148-4923164
42	FOXP2	chr7:4922910-4923628	PFSK-1	brain:	n/a	n/a
43	THAP1	chr7:4922910-4923276	K562	blood:	n/a	n/a
44	JUND	chr7:4922930-4923698	K562	blood:	n/a	chr7:4923341-4923350
45	SIN3AK20	chr7:4922889-4923424	K562	blood:	n/a	n/a
46	POLR2A	chr7:4923064-4923316	MCF-7	breast:	n/a	n/a
47	MAX	chr7:4922877-4923694	K562	blood:	n/a	chr7:4923127-4923137 chr7:4923549-4923559 chr7:4923057-4923066 chr7:4923061-4923070 chr7:4922912-4922921
48	RCOR1	chr7:4923034-4923696	K562	blood:	n/a	n/a
49	CTCF	chr7:4921537-4924514	SK-N-SH	brain:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4922058-4922071 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923020-4923030 chr7:4923545-4923558 chr7:4923748-4923761 chr7:4923319-4923332 chr7:4923314-4923332 chr7:4921846-4921859
50	CTCF	chr7:4922990-4923677	H1-hESC	embryonic stem cell:	n/a	chr7:4923315-4923331 chr7:4923542-4923560 chr7:4923508-4923521 chr7:4923507-4923523 chr7:4923506-4923524 chr7:4923316-4923329 chr7:4923508-4923521 chr7:4923440-4923453 chr7:4923316-4923329 chr7:4923020-4923030 chr7:4923545-4923558 chr7:4923319-4923332 chr7:4923314-4923332

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4923140-4923190	Hela-S3	cervix:	n/a
2	chr7:4923140-4923190	GM06990	blood:	n/a
3	chr7:4923140-4923190	HAEpiC	amniotic membrane:	n/a
4	chr7:4923140-4923190	GM12892	blood:	n/a
5	chr7:4923140-4923190	SK-N-SH	brain:	n/a
6	chr7:4923140-4923190	IMR90	lung:	fetal
7	chr7:4923140-4923190	SAEC	small airway:	n/a
8	chr7:4923140-4923190	HEK293	kidney:	embryo
9	chr7:4923140-4923190	NH-A	brain:	n/a
10	chr7:4923140-4923190	U87	brain:	n/a
11	chr7:4923140-4923190	HEEpiC	esophagus:	n/a
12	chr7:4923140-4923190	HUVEC	blood vessel:	n/a
13	chr7:4923140-4923190	PrEC	prostate:	n/a
14	chr7:4923140-4923190	PFSK-1	brain:	n/a
15	chr7:4923140-4923190	HCF	heart:	n/a
16	chr7:4923140-4923190	AG09319	gingival:	n/a
17	chr7:4923140-4923190	RPTEC	kidney:	n/a
18	chr7:4923140-4923190	BE2_C	brain:	n/a
19	chr7:4923140-4923190	HNPCEpiC	eye:	n/a
20	chr7:4923140-4923190	AG04450	lung:	fetal
21	chr7:4923140-4923190	Caco-2	colon:	n/a
22	chr7:4923140-4923190	NB4	blood:	n/a
23	chr7:4923140-4923190	T-47D	breast:	n/a
24	chr7:4923140-4923190	NHDF-neo	bronchial:	n/a
25	chr7:4923140-4923190	ovcar-3	ovarian:	n/a
26	chr7:4923140-4923190	GM12878	blood:	n/a
27	chr7:4923140-4923190	HRE	kidney:	n/a
28	chr7:4923140-4923190	Jurkat	blood:	n/a
29	chr7:4923140-4923190	GM12891	blood:	n/a
30	chr7:4923140-4923190	AG04449	skin:	fetal
31	chr7:4923140-4923190	MCF-7	breast:	n/a
32	chr7:4923140-4923190	SK-N-MC	brain:	n/a
33	chr7:4923140-4923190	H1-hESC	embryonic stem cell:	embryo
34	chr7:4923140-4923190	SKMC	muscle:	n/a
35	chr7:4923140-4923190	K562	blood:	n/a
36	chr7:4923140-4923190	NT2-D1	testis:	n/a
37	chr7:4923140-4923190	HRCEpiC	kidney:	n/a
38	chr7:4923140-4923190	ECC-1	luminal epithelium:	n/a
39	chr7:4923140-4923190	HIPEpiC	eye:	n/a
40	chr7:4923140-4923190	HMEC	breast:	n/a
41	chr7:4923140-4923190	HCM	heart:	n/a
42	chr7:4923140-4923190	HCT-116	colon:	n/a
43	chr7:4923140-4923190	NHBE	bronchial:	n/a
44	chr7:4923140-4923190	AoSMC	blood vessel:	n/a
45	chr7:4923140-4923190	Hepatocyte	liver:	n/a
46	chr7:4923140-4923190	LNCaP	prostate:	n/a
47	chr7:4923140-4923190	HepG2	liver:	n/a
48	chr7:4923140-4923190	GM19239	blood:	n/a
49	chr7:4923140-4923190	AG10803	skin:	n/a
50	chr7:4923140-4923190	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:4920954..4923771-chr7:5084405..5086180,2	K562	blood:
2	chr7:4923091..4923826-chr7:5013336..5013934,3	K562	blood:

Variant related genes	Relation type
RADIL	TF binding region
RADIL	CpG island
ENSG00000146587	Chromatin interaction
ENSG00000272968	Chromatin interaction
ENSG00000196204	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529538	chr7:4509189-5151503	Enhancers Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv530968	chr7:4572250-5418004	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv1031697	chr7:4677463-5241790	Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
4	nsv538704	chr7:4677463-5241790	Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Weak transcription Bivalent Enhancer 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 miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
5	nsv887378	chr7:4730535-4929721	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
6	nsv887380	chr7:4760124-4929721	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
7	nsv823994	chr7:4792385-4928328	Weak transcription Genic enhancers Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
8	nsv8033	chr7:4802287-5086597	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
9	nsv1022678	chr7:4810626-5113387	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
10	nsv538705	chr7:4810626-5113387	Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
11	nsv528748	chr7:4820581-5010993	Enhancers Strong transcription Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
12	nsv1021170	chr7:4831361-5058033	Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
13	nsv538706	chr7:4831361-5058033	Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
14	nsv1025467	chr7:4850447-5021443	ZNF genes & repeats Bivalent/Poised TSS Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
15	nsv605979	chr7:4854592-4944514	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
16	nsv1021999	chr7:4862082-5003190	Genic enhancers Enhancers Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
17	nsv538707	chr7:4862082-5003190	Weak transcription Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
18	nsv1033855	chr7:4862677-5069764	Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
19	nsv605980	chr7:4876057-5003373	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
20	nsv869165	chr7:4889618-5799719	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	352 gene(s)	inside rSNPs	diseases
21	nsv971151	chr7:4915196-4928162	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
22	esv3434811	chr7:4922326-4924674	Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4921400-4923400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr7:4921400-4923400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr7:4921400-4923400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:4921400-4923400	Active TSS	Right Atrium	heart
5	chr7:4921600-4923200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr7:4921600-4923200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr7:4921600-4923400	Active TSS	H9 Cell Line	embryonic stem cell
8	chr7:4921600-4923400	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
9	chr7:4921600-4923400	Active TSS	Left Ventricle	heart
10	chr7:4921600-4923600	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
11	chr7:4921600-4923800	Active TSS	Aorta	Aorta
12	chr7:4921600-4923800	Active TSS	Brain Angular Gyrus	brain
13	chr7:4921800-4923200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
14	chr7:4921800-4923200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
15	chr7:4921800-4923200	Active TSS	NHDF-Ad	bronchial
16	chr7:4921800-4923400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr7:4921800-4923400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr7:4921800-4923400	Active TSS	Brain Hippocampus Middle	brain
19	chr7:4921800-4923400	Active TSS	Lung	lung
20	chr7:4921800-4923400	Active TSS	Psoas Muscle	Psoas
21	chr7:4921800-4923600	Active TSS	Ovary	ovary
22	chr7:4921800-4923800	Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr7:4922000-4923400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr7:4922000-4923400	Active TSS	Pancreatic Islets	Pancreatic Islet
25	chr7:4922000-4923600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr7:4922200-4923200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr7:4922200-4923200	Active TSS	Rectal Smooth Muscle	rectum
28	chr7:4922200-4923400	Active TSS	HUES6 Cell Line	embryonic stem cell
29	chr7:4922200-4923400	Active TSS	Brain Inferior Temporal Lobe	brain
30	chr7:4922200-4923400	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
31	chr7:4922200-4923600	Bivalent Enhancer	Primary B cells from cord blood	blood
32	chr7:4922200-4923800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr7:4922400-4923400	Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr7:4922400-4923400	Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr7:4922400-4923600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
36	chr7:4922400-4923600	Bivalent/Poised TSS	Thymus	Thymus
37	chr7:4922400-4923800	Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr7:4922400-4923800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
39	chr7:4922600-4923200	Flanking Active TSS	Primary hematopoietic stem cells	blood
40	chr7:4922600-4923200	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
41	chr7:4922600-4923200	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr7:4922600-4923200	Enhancers	Gastric	stomach
43	chr7:4922600-4923200	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
44	chr7:4922600-4923200	Flanking Active TSS	Stomach Smooth Muscle	stomach
45	chr7:4922600-4923200	Active TSS	HSMMtube	muscle
46	chr7:4922600-4923400	Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr7:4922600-4923400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr7:4922600-4923400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr7:4922600-4923400	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
50	chr7:4922600-4923400	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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