Variant report

Variant	rs852536
Chromosome Location	chr7:5594385-5594386
allele	A/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	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
2	GATA1	chr7:5594057-5596635	K562	blood:	n/a	chr7:5595745-5595752 chr7:5594774-5594783 chr7:5595740-5595749
3	MXI1	chr7:5593993-5596851	SK-N-SH	brain:	n/a	n/a
4	CEBPD	chr7:5594087-5596292	K562	blood:	n/a	n/a
5	POLR2A	chr7:5594213-5594500	GM12878	blood:	n/a	n/a
6	STAT5A	chr7:5594339-5596998	GM12878	blood:	n/a	chr7:5596281-5596293 chr7:5596276-5596288 chr7:5596257-5596269 chr7:5596111-5596118
7	CBX3	chr7:5593922-5594929	K562	blood:	n/a	n/a
8	MAX	chr7:5593983-5596790	A549	lung:	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
9	NFATC1	chr7:5594335-5594806	GM12878	blood:	n/a	n/a
10	POLR2A	chr7:5594093-5596833	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr7:5594228-5596651	Hela-S3	cervix:	n/a	n/a
12	ZNF143	chr7:5594091-5594806	K562	blood:	n/a	n/a
13	POLR2A	chr7:5594160-5594386	MCF-7	breast:	n/a	n/a
14	POLR2A	chr7:5594288-5594853	HepG2	liver:	n/a	n/a
15	MAX	chr7:5594092-5596705	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
16	TCF7L2	chr7:5594232-5594719	Hela-S3	cervix:	n/a	n/a
17	FOXA2	chr7:5594234-5594779	A549	lung:	n/a	n/a
18	POLR2A	chr7:5594384-5594802	GM12891	blood:	n/a	n/a
19	MTA3	chr7:5593891-5599216	GM12878	blood:	n/a	n/a
20	RCOR1	chr7:5593908-5596961	IMR90	lung:	n/a	n/a
21	POLR2A	chr7:5594204-5594801	GM12891	blood:	n/a	n/a
22	PML	chr7:5594365-5594962	K562	blood:	n/a	n/a
23	TRIM28	chr7:5594353-5594975	K562	blood:	n/a	n/a
24	POLR2A	chr7:5594221-5596937	MCF10A-Er-Src	breast:	n/a	n/a
25	GATA2	chr7:5594158-5594905	K562	blood:	n/a	chr7:5594774-5594783
26	MAZ	chr7:5594377-5596746	Hela-S3	cervix:	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 chr7:5596285-5596295
27	ZNF143	chr7:5594265-5596064	Hela-S3	cervix:	n/a	chr7:5595562-5595572 chr7:5595559-5595577 chr7:5595818-5595828 chr7:5594913-5594931
28	GABPA	chr7:5594102-5594448	K562	blood:	n/a	n/a
29	KAP1	chr7:5594141-5594636	K562	blood:	n/a	n/a
30	EP300	chr7:5594221-5596484	K562	blood:	n/a	chr7:5596094-5596110 chr7:5594988-5595004 chr7:5595866-5595882 chr7:5594653-5594662 chr7:5594989-5595005
31	E2F6	chr7:5594362-5596408	A549	lung:	n/a	chr7:5595715-5595727 chr7:5594943-5594953 chr7:5595562-5595572 chr7:5596215-5596229
32	PML	chr7:5594155-5596865	GM12878	blood:	n/a	n/a
33	POLR2A	chr7:5593981-5594869	HCT-116	colon:	n/a	n/a
34	MAZ	chr7:5594298-5596819	GM12878	blood:	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
35	STAT5A	chr7:5594154-5594954	K562	blood:	n/a	chr7:5594332-5594344
36	ZMIZ1	chr7:5594315-5596456	K562	blood:	n/a	n/a
37	RCOR1	chr7:5594065-5596606	K562	blood:	n/a	n/a
38	CREB1	chr7:5594114-5596572	HepG2	liver:	n/a	n/a
39	TCF12	chr7:5593931-5597250	A549	lung:	n/a	n/a
40	POLR2A	chr7:5593989-5596146	K562	blood:	n/a	n/a
41	POLR2A	chr7:5593940-5598939	GM12878	blood:	n/a	n/a
42	FOXA1	chr7:5594286-5594536	T-47D	breast:	n/a	n/a
43	BHLHE40	chr7:5594118-5596200	K562	blood:	n/a	chr7:5596093-5596109 chr7:5596090-5596106 chr7:5594727-5594743 chr7:5595856-5595872
44	BACH1	chr7:5594355-5595142	K562	blood:	n/a	n/a
45	TBP	chr7:5594194-5596710	K562	blood:	n/a	chr7:5595238-5595249
46	MYC	chr7:5594140-5596630	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
47	TAL1	chr7:5594111-5596182	K562	blood:	n/a	n/a
48	TEAD4	chr7:5594054-5596173	K562	blood:	n/a	n/a
49	CHD2	chr7:5594275-5594888	K562	blood:	n/a	n/a
50	RCOR1	chr7:5594075-5596697	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:5593112..5594944-chr7:5719558..5721902,2	MCF-7	breast:
2	chr7:5456513..5458866-chr7:5593273..5595987,2	MCF-7	breast:
3	chr7:5581518..5584209-chr7:5593146..5596180,3	MCF-7	breast:
4	chr11:62608625..62609155-chr7:5594288..5595164,2	NB4	blood:
5	chr7:5558806..5574463-chr7:5583405..5604290,160	MCF-7	breast:
6	chr7:5532197..5537592-chr7:5593884..5603950,17	MCF-7	breast:
7	chr7:5579007..5580984-chr7:5593985..5595779,2	MCF-7	breast:
8	chr7:5464910..5469932-chr7:5594160..5600416,10	MCF-7	breast:
9	chr6:74229955..74230681-chr7:5594286..5595068,2	Hela-S3	cervix:
10	chr7:5551753..5555420-chr7:5594196..5597835,12	MCF-7	breast:
11	chr7:5320876..5323087-chr7:5592627..5594710,2	K562	blood:
12	chr7:5538597..5541338-chr7:5594039..5595766,2	K562	blood:
13	chr7:5458987..5464555-chr7:5593156..5597256,5	K562	blood:
14	chr7:5462448..5464237-chr7:5593422..5596155,2	MCF-7	breast:
15	chr7:5531499..5540573-chr7:5594200..5602257,20	MCF-7	breast:
16	chr7:5464575..5468127-chr7:5593379..5596799,6	K562	blood:
17	chr7:2561342..2564063-chr7:5594340..5595887,2	MCF-7	breast:
18	chr7:5463649..5470093-chr7:5593803..5597245,7	MCF-7	breast:

Variant related genes	Relation type
ENSG00000272719	TF binding region
ENSG00000272953	Chromatin interaction
ENSG00000207973	Chromatin interaction
ENSG00000182095	Chromatin interaction
ENSG00000237738	Chromatin interaction
ENSG00000155034	Chromatin interaction
ENSG00000164638	Chromatin interaction
ENSG00000234432	Chromatin interaction
ENSG00000075624	Chromatin interaction
ENSG00000273084	Chromatin interaction
ENSG00000188365	Chromatin interaction
ENSG00000263900	Chromatin interaction
ENSG00000106003	Chromatin interaction
ENSG00000241269	Chromatin interaction

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs1628786	1.00[AMR][1000 genomes]
rs1725186	1.00[AMR][1000 genomes]
rs1990835	0.83[AMR][1000 genomes]
rs2161012	0.83[AMR][1000 genomes]
rs2693951	1.00[AMR][1000 genomes]
rs2908421	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4720636	0.83[AMR][1000 genomes]
rs4724714	0.83[AMR][1000 genomes]
rs710939	1.00[AMR][1000 genomes]
rs710940	1.00[AMR][1000 genomes]
rs710942	1.00[AMR][1000 genomes]
rs852260	0.83[AMR][1000 genomes]
rs852262	1.00[AMR][1000 genomes]
rs852264	1.00[AMR][1000 genomes]
rs852377	0.83[AMR][1000 genomes]
rs852381	1.00[AMR][1000 genomes]
rs852383	1.00[AMR][1000 genomes]
rs852398	1.00[AMR][1000 genomes]
rs852399	1.00[AMR][1000 genomes]
rs852401	1.00[AMR][1000 genomes]
rs852404	1.00[AMR][1000 genomes]
rs852407	1.00[AMR][1000 genomes]
rs852408	1.00[AMR][1000 genomes]
rs852412	1.00[AMR][1000 genomes]
rs852413	1.00[AMR][1000 genomes]
rs852416	1.00[AMR][1000 genomes]
rs852419	1.00[AMR][1000 genomes]
rs852437	0.85[AMR][1000 genomes]
rs852440	0.85[AMR][1000 genomes]
rs852443	1.00[AMR][1000 genomes]
rs852449	1.00[AMR][1000 genomes]
rs852451	1.00[AMR][1000 genomes]
rs852458	1.00[AMR][1000 genomes]
rs852462	0.85[AMR][1000 genomes]
rs852465	1.00[AMR][1000 genomes]
rs852475	0.85[AMR][1000 genomes]
rs852476	1.00[AMR][1000 genomes]
rs852480	1.00[AMR][1000 genomes]
rs852487	0.85[AMR][1000 genomes]
rs852490	1.00[AMR][1000 genomes]
rs852495	1.00[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs852497	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs852501	0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs852503	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs852504	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs852509	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs852511	0.83[EUR][1000 genomes]
rs852513	0.90[ASN][1000 genomes]
rs852518	1.00[AMR][1000 genomes]
rs852523	1.00[AMR][1000 genomes]
rs852524	1.00[AMR][1000 genomes]
rs852525	1.00[AMR][1000 genomes]
rs852528	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs852540	1.00[JPT][hapmap]
rs852541	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs852543	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs852544	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs941016	0.85[AMR][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:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5572600-5594600	Weak transcription	Right Atrium	heart
2	chr7:5588800-5595000	Enhancers	Placenta	Placenta
3	chr7:5589000-5594400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr7:5589400-5594400	Weak transcription	HUVEC	blood vessel
5	chr7:5589400-5595000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr7:5589400-5595200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr7:5589600-5594400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr7:5589600-5594400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr7:5589600-5594400	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr7:5589600-5594400	Weak transcription	NHDF-Ad	bronchial
11	chr7:5589600-5594600	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr7:5589600-5594800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr7:5589600-5595000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr7:5589600-5595000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr7:5589600-5595200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr7:5589800-5594400	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr7:5590600-5594400	Weak transcription	Gastric	stomach
18	chr7:5591600-5595000	Enhancers	Fetal Intestine Large	intestine
19	chr7:5591800-5594400	Enhancers	Colonic Mucosa	Colon
20	chr7:5591800-5595000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr7:5592400-5594400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr7:5592400-5594600	Flanking Active TSS	Hela-S3	cervix
23	chr7:5592400-5595000	Enhancers	Liver	Liver
24	chr7:5592600-5594800	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr7:5592600-5595000	Enhancers	Stomach Mucosa	stomach
26	chr7:5592800-5594400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr7:5592800-5594600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr7:5593000-5594400	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr7:5593000-5595000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr7:5593000-5595000	Enhancers	Rectal Mucosa Donor 29	rectum
31	chr7:5593000-5595000	Enhancers	NHEK	skin
32	chr7:5593200-5594400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr7:5593200-5594400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr7:5593200-5594400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr7:5593200-5595200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr7:5593400-5594400	Enhancers	HepG2	liver
37	chr7:5593400-5594400	Weak transcription	HMEC	breast
38	chr7:5593400-5595000	Weak transcription	HSMM	muscle
39	chr7:5593400-5595200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr7:5593600-5594400	Enhancers	Fetal Muscle Leg	muscle
41	chr7:5593600-5595000	Weak transcription	HSMMtube	muscle
42	chr7:5593800-5594400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr7:5593800-5594600	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr7:5594000-5594400	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr7:5594000-5594400	Enhancers	Colon Smooth Muscle	Colon
46	chr7:5594000-5594400	Enhancers	Fetal Intestine Small	intestine
47	chr7:5594000-5594400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
48	chr7:5594000-5594600	Flanking Active TSS	Rectal Smooth Muscle	rectum
49	chr7:5594000-5595000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr7:5594000-5595000	Enhancers	Primary T cells fromperipheralblood	blood

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