Variant report

Variant	rs852534
Chromosome Location	chr7:5595793-5595794
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	TCF7L2	chr7:5595394-5596355	HCT-116	colon:	n/a	chr7:5595742-5595751
2	SRF	chr7:5595464-5596356	ECC-1	luminal epithelium:	n/a	chr7:5596040-5596058 chr7:5596041-5596055 chr7:5595875-5595885 chr7:5596043-5596057 chr7:5595549-5595559 chr7:5596038-5596056 chr7:5596285-5596295 chr7:5596043-5596060 chr7:5596043-5596054
3	POLR2A	chr7:5595327-5595932	HepG2	liver:	n/a	n/a
4	MAX	chr7:5594492-5596702	NB4	blood:	n/a	chr7:5594947-5594957 chr7:5595268-5595284 chr7:5594716-5594727 chr7:5596275-5596285 chr7:5595566-5595576 chr7:5594719-5594728 chr7:5595011-5595021 chr7:5595024-5595033 chr7:5595212-5595222 chr7:5596285-5596295
5	E2F4	chr7:5594506-5595841	K562	blood:	n/a	chr7:5595715-5595727 chr7:5594943-5594953 chr7:5595562-5595572
6	POLR2A	chr7:5594528-5596771	GM18505	blood:	n/a	n/a
7	NFATC1	chr7:5594849-5595883	GM12878	blood:	n/a	n/a
8	PBX3	chr7:5595389-5595919	A549	lung:	n/a	n/a
9	ELK1	chr7:5595539-5595800	Hela-S3	cervix:	n/a	n/a
10	NR2F2	chr7:5595008-5595955	K562	blood:	n/a	n/a
11	REST	chr7:5595437-5596011	PANC-1	pancreas:	n/a	chr7:5595857-5595870
12	RUNX3	chr7:5594958-5596729	GM12878	blood:	n/a	n/a
13	MAZ	chr7:5593980-5596833	IMR90	lung:	n/a	chr7:5594947-5594957 chr7:5596798-5596808 chr7:5595268-5595284 chr7:5594716-5594727 chr7:5596275-5596285 chr7:5595566-5595576 chr7:5594719-5594728 chr7:5595011-5595021 chr7:5595024-5595033 chr7:5596285-5596295
14	GATA1	chr7:5594057-5596635	K562	blood:	n/a	chr7:5595745-5595752 chr7:5594774-5594783 chr7:5595740-5595749
15	ELF1	chr7:5595642-5595954	K562	blood:	n/a	n/a
16	RUNX3	chr7:5594856-5596662	GM12878	blood:	n/a	n/a
17	HA-E2F1	chr7:5595771-5596414	Hela-S3	cervix:	n/a	chr7:5596215-5596229
18	POLR2A	chr7:5595037-5596572	H1-hESC	embryonic stem cell:	n/a	n/a
19	MXI1	chr7:5593993-5596851	SK-N-SH	brain:	n/a	n/a
20	CCNT2	chr7:5594459-5596546	K562	blood:	n/a	chr7:5595560-5595569 chr7:5595815-5595824 chr7:5595723-5595732 chr7:5596363-5596372 chr7:5594686-5594706 chr7:5596261-5596270
21	POLR2A	chr7:5594953-5596754	U87	brain:	n/a	n/a
22	POLR2A	chr7:5595078-5596223	HepG2	liver:	n/a	n/a
23	MYC	chr7:5594492-5596688	K562	blood:	n/a	chr7:5594947-5594957 chr7:5595268-5595284 chr7:5594716-5594727 chr7:5596275-5596285 chr7:5595566-5595576 chr7:5594719-5594728 chr7:5595011-5595021 chr7:5595024-5595033 chr7:5595212-5595222 chr7:5596285-5596295
24	CTCF	chr7:5595700-5595850	HRPEpiC	eye:	n/a	n/a
25	STAT3	chr7:5595427-5597048	MCF10A-Er-Src	breast:	n/a	chr7:5596281-5596293 chr7:5596276-5596288 chr7:5596257-5596269 chr7:5596111-5596118
26	UBTF	chr7:5595642-5596565	K562	blood:	n/a	n/a
27	PBX3	chr7:5595200-5596013	A549	lung:	n/a	n/a
28	POLR2A	chr7:5595543-5595903	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr7:5594926-5596858	PANC-1	pancreas:	n/a	n/a
30	POLR2A	chr7:5594861-5596403	HL-60	blood:	n/a	n/a
31	ATF2	chr7:5595083-5595885	H1-hESC	embryonic stem cell:	n/a	n/a
32	TAF7	chr7:5594932-5596756	H1-hESC	embryonic stem cell:	n/a	n/a
33	TCF3	chr7:5595784-5596245	GM12878	blood:	n/a	n/a
34	EGR1	chr7:5595216-5596623	K562	blood:	n/a	chr7:5596256-5596269 chr7:5596211-5596224 chr7:5595328-5595341 chr7:5595328-5595341 chr7:5595567-5595577 chr7:5596286-5596296 chr7:5595329-5595339 chr7:5596213-5596223 chr7:5596276-5596286 chr7:5595327-5595342 chr7:5595562-5595575
35	TBL1XR1	chr7:5595099-5596176	K562	blood:	n/a	n/a
36	POLR2A	chr7:5595008-5596754	U87	brain:	n/a	n/a
37	ELF1	chr7:5594831-5596691	GM12878	blood:	n/a	chr7:5595544-5595556 chr7:5596286-5596298 chr7:5596141-5596153
38	RELA	chr7:5595673-5596760	GM19193	blood:	n/a	n/a
39	CTBP2	chr7:5595064-5596430	H1-hESC	embryonic stem cell:	n/a	n/a
40	POLR2A	chr7:5594510-5596744	HCT-116	colon:	n/a	n/a
41	POLR2A	chr7:5594924-5596225	GM12891	blood:	n/a	n/a
42	POLR2A	chr7:5594497-5596721	K562	blood:	n/a	n/a
43	STAT3	chr7:5595589-5596612	MCF10A-Er-Src	breast:	n/a	chr7:5596281-5596293 chr7:5596276-5596288 chr7:5596257-5596269 chr7:5596111-5596118
44	RCOR1	chr7:5594998-5596636	Hela-S3	cervix:	n/a	n/a
45	HCFC1	chr7:5594428-5596483	K562	blood:	n/a	n/a
46	STAT3	chr7:5595428-5596828	MCF10A-Er-Src	breast:	n/a	chr7:5596281-5596293 chr7:5596276-5596288 chr7:5596257-5596269 chr7:5596111-5596118
47	TBL1XR1	chr7:5594434-5595840	K562	blood:	n/a	n/a
48	CEBPD	chr7:5594087-5596292	K562	blood:	n/a	n/a
49	YY1	chr7:5595262-5596399	A549	lung:	n/a	chr7:5596205-5596216 chr7:5596278-5596289 chr7:5596207-5596221 chr7:5595569-5595580 chr7:5596210-5596219 chr7:5595543-5595557
50	POLR2A	chr7:5595441-5595959	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:5595299..5597821-chr7:5720043..5723343,4	MCF-7	breast:
2	chr7:5570152..5570887-chr7:5595377..5596139,2	MCF-7	breast:
3	chr7:5533565..5537610-chr7:5594791..5600448,10	K562	blood:
4	chr7:5595437..5596087-chr7:73668110..73668941,2	Hela-S3	cervix:
5	chr7:5456513..5458866-chr7:5593273..5595987,2	MCF-7	breast:
6	chr11:64085656..64086417-chr7:5595594..5596260,2	Hela-S3	cervix:
7	chr7:5581518..5584209-chr7:5593146..5596180,3	MCF-7	breast:
8	chr14:70233834..70234634-chr7:5595667..5596496,2	NB4	blood:
9	chr3:73159770..73160591-chr7:5595780..5596290,2	Hela-S3	cervix:
10	chr7:5569416..5570319-chr7:5595634..5596437,2	Hela-S3	cervix:
11	chr7:5558806..5574463-chr7:5583405..5604290,160	MCF-7	breast:
12	chr7:5595573..5597650-chr7:5633861..5636258,2	MCF-7	breast:
13	chr7:5532197..5537592-chr7:5593884..5603950,17	MCF-7	breast:
14	chr7:5464910..5469932-chr7:5594160..5600416,10	MCF-7	breast:
15	chr7:5463546..5466372-chr7:5594694..5597201,2	K562	blood:
16	chr7:5551753..5555420-chr7:5594196..5597835,12	MCF-7	breast:
17	chr11:355444..356041-chr7:5595616..5596299,2	Hela-S3	cervix:
18	chr15:76628598..76629501-chr7:5595167..5596070,2	NB4	blood:
19	chr1:24306202..24306896-chr7:5595367..5596353,2	Hela-S3	cervix:
20	chr17:72199606..72200171-chr7:5595411..5596166,2	Hela-S3	cervix:
21	chr7:5533960..5534879-chr7:5595242..5596197,3	MCF-7	breast:
22	chr7:5458987..5464555-chr7:5593156..5597256,5	K562	blood:
23	chr7:5462448..5464237-chr7:5593422..5596155,2	MCF-7	breast:
24	chr7:5570357..5570899-chr7:5595458..5596005,2	NB4	blood:
25	chr7:5531499..5540573-chr7:5594200..5602257,20	MCF-7	breast:
26	chr1:201978819..201979809-chr7:5595784..5596642,2	Hela-S3	cervix:
27	chr7:5464575..5468127-chr7:5593379..5596799,6	K562	blood:
28	chr7:5570027..5570789-chr7:5595635..5596381,2	HCT-116	colon:
29	chr7:2561342..2564063-chr7:5594340..5595887,2	MCF-7	breast:
30	chr7:5463649..5470093-chr7:5593803..5597245,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000272719	TF binding region
ENSG00000228974	TF binding region
ENSG00000106003	Chromatin interaction
ENSG00000075618	Chromatin interaction
ENSG00000234678	Chromatin interaction
ENSG00000172809	Chromatin interaction
ENSG00000155034	Chromatin interaction
ENSG00000223247	Chromatin interaction
ENSG00000163435	Chromatin interaction
ENSG00000188365	Chromatin interaction
ENSG00000207973	Chromatin interaction
ENSG00000188529	Chromatin interaction
ENSG00000272953	Chromatin interaction
ENSG00000075624	Chromatin interaction
ENSG00000237738	Chromatin interaction
ENSG00000100650	Chromatin interaction
ENSG00000263900	Chromatin interaction
ENSG00000241269	Chromatin interaction
ENSG00000182095	Chromatin interaction
ENSG00000273084	Chromatin interaction
ENSG00000234432	Chromatin interaction
ENSG00000159556	Chromatin interaction
ENSG00000049541	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs2908421	0.85[ASN][1000 genomes]
rs852492	0.83[ASN][1000 genomes]
rs852496	0.80[ASN][1000 genomes]
rs852501	0.85[ASN][1000 genomes]
rs852503	0.85[ASN][1000 genomes]
rs852504	0.85[ASN][1000 genomes]
rs852509	0.85[ASN][1000 genomes]
rs852513	0.81[ASN][1000 genomes]
rs852528	0.85[ASN][1000 genomes]
rs852535	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs852537	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs852538	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs852539	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs852540	1.00[ASN][1000 genomes]
rs852541	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	nsv530979	chr7:5101631-5864814	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
3	nsv530981	chr7:5157150-5920006	Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	348 gene(s)	inside rSNPs	diseases
4	esv1814049	chr7:5314993-5675131	Active TSS Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers 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	333 gene(s)	inside rSNPs	diseases
5	esv1820266	chr7:5332088-5665173	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	332 gene(s)	inside rSNPs	diseases
6	nsv530983	chr7:5370746-6070852	Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	368 gene(s)	inside rSNPs	diseases
7	nsv887404	chr7:5402606-5667645	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	331 gene(s)	inside rSNPs	diseases
8	nsv916391	chr7:5417945-5889565	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	336 gene(s)	inside rSNPs	diseases
9	nsv887407	chr7:5432672-5605130	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	302 gene(s)	inside rSNPs	diseases
10	nsv887408	chr7:5432672-5667645	Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised 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 miRNA target site	331 gene(s)	inside rSNPs	diseases
11	nsv830890	chr7:5464933-5705158	Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
12	nsv533108	chr7:5488018-6316581	Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	390 gene(s)	inside rSNPs	diseases
13	nsv887413	chr7:5521468-5607884	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	279 gene(s)	inside rSNPs	diseases
14	nsv1025434	chr7:5537571-5705283	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	297 gene(s)	inside rSNPs	diseases
15	nsv482449	chr7:5557585-5743673	Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	294 gene(s)	inside rSNPs	diseases
16	nsv1033556	chr7:5565080-6186815	Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	357 gene(s)	inside rSNPs	diseases
17	nsv538710	chr7:5565080-6186815	Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	357 gene(s)	inside rSNPs	diseases
18	nsv887414	chr7:5584934-5667645	Flanking Bivalent TSS/Enh Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
19	nsv887415	chr7:5584934-5675305	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
20	nsv887416	chr7:5584934-5695259	Genic enhancers Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	68 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5594200-5595800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr7:5594200-5595800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
3	chr7:5594200-5596000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr7:5594400-5595800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr7:5594400-5596000	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:5594400-5596000	Bivalent Enhancer	Fetal Brain Male	brain
7	chr7:5594400-5596400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
8	chr7:5594400-5596800	Active TSS	H9 Cell Line	embryonic stem cell
9	chr7:5594400-5596800	Flanking Active TSS	Fetal Muscle Leg	muscle
10	chr7:5594600-5595800	Enhancers	Fetal Heart	heart
11	chr7:5594600-5596400	Active TSS	Ovary	ovary
12	chr7:5594600-5596600	Active TSS	HUES48 Cell Line	embryonic stem cell
13	chr7:5594600-5596600	Active TSS	iPS-15b Cell Line	embryonic stem cell
14	chr7:5594600-5596600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr7:5594600-5596600	Active TSS	Colon Smooth Muscle	Colon
16	chr7:5594600-5596600	Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr7:5594600-5596800	Active TSS	Psoas Muscle	Psoas
18	chr7:5594800-5596000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr7:5594800-5596600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr7:5594800-5596600	Active TSS	Aorta	Aorta
21	chr7:5594800-5596800	Active TSS	Small Intestine	intestine
22	chr7:5594800-5598600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
23	chr7:5594800-5598800	Flanking Active TSS	Primary B cells from peripheral blood	blood
24	chr7:5594800-5599000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
25	chr7:5595000-5595800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr7:5595000-5595800	Flanking Active TSS	Primary B cells from cord blood	blood
27	chr7:5595000-5595800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr7:5595000-5595800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr7:5595000-5595800	Flanking Active TSS	Adipose Nuclei	Adipose
30	chr7:5595000-5595800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
31	chr7:5595000-5595800	Flanking Active TSS	Brain Hippocampus Middle	brain
32	chr7:5595000-5595800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
33	chr7:5595000-5595800	Flanking Active TSS	Fetal Intestine Large	intestine
34	chr7:5595000-5595800	Flanking Active TSS	Fetal Muscle Trunk	muscle
35	chr7:5595000-5595800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
36	chr7:5595000-5595800	Flanking Bivalent TSS/Enh	Thymus	Thymus
37	chr7:5595000-5595800	Flanking Active TSS	Spleen	Spleen
38	chr7:5595000-5595800	Flanking Active TSS	GM12878-XiMat	blood
39	chr7:5595000-5595800	Flanking Active TSS	HUVEC	blood vessel
40	chr7:5595000-5596000	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr7:5595000-5596000	Flanking Active TSS	Primary hematopoietic stem cells	blood
42	chr7:5595000-5596000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
43	chr7:5595000-5596000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr7:5595000-5596000	Flanking Active TSS	Liver	Liver
45	chr7:5595000-5596000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
46	chr7:5595000-5596200	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr7:5595000-5596200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
48	chr7:5595000-5596400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:5595000-5596600	Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr7:5595000-5596600	Active TSS	iPS-20b Cell Line	embryonic stem cell

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