Variant report

Variant	rs7757984
Chromosome Location	chr6:150208651-150208652
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	JUND	chr6:150208591-150208787	HepG2	liver:	n/a	chr6:150208601-150208613 chr6:150208696-150208703 chr6:150208766-150208774 chr6:150208693-150208704 chr6:150208695-150208703 chr6:150208695-150208703 chr6:150208764-150208776
2	GATA1	chr6:150208361-150209070	PBDE	blood:	n/a	chr6:150208596-150208606 chr6:150208597-150208604 chr6:150208598-150208615 chr6:150208597-150208606 chr6:150208595-150208607
3	RFX5	chr6:150208274-150208866	Hela-S3	cervix:	n/a	n/a
4	ARID3A	chr6:150208597-150208770	HepG2	liver:	n/a	n/a
5	TBP	chr6:150208475-150208982	Hela-S3	cervix:	n/a	n/a
6	E2F4	chr6:150208545-150208835	MCF10A-Er-Src	breast:	n/a	n/a
7	STAT3	chr6:150208563-150208845	MCF10A-Er-Src	breast:	n/a	n/a
8	MYC	chr6:150208500-150208881	MCF10A-Er-Src	breast:	n/a	n/a
9	CEBPB	chr6:150208451-150208895	A549	lung:	n/a	chr6:150208872-150208884
10	GATA3	chr6:150208263-150209032	A549	lung:	n/a	chr6:150208596-150208606 chr6:150208597-150208604 chr6:150208598-150208615 chr6:150208597-150208606 chr6:150208595-150208607
11	TCF12	chr6:150208545-150208881	A549	lung:	n/a	n/a
12	JUND	chr6:150208464-150208853	A549	lung:	n/a	chr6:150208601-150208613 chr6:150208696-150208703 chr6:150208766-150208774 chr6:150208693-150208704 chr6:150208695-150208703 chr6:150208695-150208703 chr6:150208764-150208776
13	SMARCC1	chr6:150208250-150211123	Hela-S3	cervix:	n/a	chr6:150208765-150208774
14	RCOR1	chr6:150208405-150208912	Hela-S3	cervix:	n/a	n/a
15	MAZ	chr6:150208561-150209000	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr6:150208551-150208696	K562	blood:	n/a	n/a
17	MAFK	chr6:150208505-150208914	Hela-S3	cervix:	n/a	chr6:150208522-150208533 chr6:150208523-150208534 chr6:150208523-150208534
18	JUND	chr6:150208323-150209057	HCT-116	colon:	n/a	chr6:150208601-150208613 chr6:150208696-150208703 chr6:150208766-150208774 chr6:150208693-150208704 chr6:150208695-150208703 chr6:150208695-150208703 chr6:150208764-150208776 chr6:150208449-150208459
19	POLR2A	chr6:150208491-150209777	Hela-S3	cervix:	n/a	n/a
20	SP1	chr6:150208380-150208978	A549	lung:	n/a	chr6:150208388-150208401
21	EP300	chr6:150208495-150208944	Hela-S3	cervix:	n/a	chr6:150208694-150208703
22	CHD2	chr6:150208397-150208944	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr6:150208507-150208841	HCT-116	colon:	n/a	n/a
24	FOSL1	chr6:150208444-150209051	HCT-116	colon:	n/a	chr6:150208601-150208613 chr6:150208696-150208703 chr6:150208766-150208774 chr6:150208695-150208703 chr6:150208695-150208703 chr6:150208764-150208776 chr6:150208449-150208459
25	SMC3	chr6:150208457-150208932	Hela-S3	cervix:	n/a	n/a
26	MAX	chr6:150208457-150208988	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr6:150208463-150208907	A549	lung:	n/a	chr6:150208872-150208884
28	FOS	chr6:150208485-150208926	MCF10A-Er-Src	breast:	n/a	chr6:150208601-150208613 chr6:150208696-150208703 chr6:150208766-150208774 chr6:150208695-150208703 chr6:150208695-150208703 chr6:150208764-150208776
29	JUND	chr6:150208368-150209091	HCT-116	colon:	n/a	chr6:150208601-150208613 chr6:150208696-150208703 chr6:150208766-150208774 chr6:150208693-150208704 chr6:150208695-150208703 chr6:150208695-150208703 chr6:150208764-150208776 chr6:150208449-150208459
30	JUND	chr6:150208498-150208802	A549	lung:	n/a	chr6:150208601-150208613 chr6:150208696-150208703 chr6:150208766-150208774 chr6:150208693-150208704 chr6:150208695-150208703 chr6:150208695-150208703 chr6:150208764-150208776
31	MAFK	chr6:150208545-150208867	IMR90	lung:	n/a	n/a
32	SP1	chr6:150208393-150209008	A549	lung:	n/a	n/a
33	POLR2A	chr6:150208138-150210950	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr6:150208490-150208915	U87	brain:	n/a	n/a
35	TCF12	chr6:150208318-150209752	A549	lung:	n/a	n/a
36	CEBPB	chr6:150208322-150209079	HCT-116	colon:	n/a	chr6:150208872-150208884
37	FOSL2	chr6:150208423-150209027	A549	lung:	n/a	chr6:150208601-150208613 chr6:150208696-150208703 chr6:150208766-150208774 chr6:150208695-150208703 chr6:150208695-150208703 chr6:150208764-150208776 chr6:150208449-150208459
38	FOSL2	chr6:150208476-150208867	A549	lung:	n/a	chr6:150208601-150208613 chr6:150208696-150208703 chr6:150208766-150208774 chr6:150208695-150208703 chr6:150208695-150208703 chr6:150208764-150208776
39	FOS	chr6:150208480-150208931	MCF10A-Er-Src	breast:	n/a	chr6:150208601-150208613 chr6:150208696-150208703 chr6:150208766-150208774 chr6:150208695-150208703 chr6:150208695-150208703 chr6:150208764-150208776
40	RAD21	chr6:150208463-150208917	Hela-S3	cervix:	n/a	n/a
41	GABPA	chr6:150208451-150208914	A549	lung:	n/a	n/a
42	ZKSCAN1	chr6:150208415-150208912	Hela-S3	cervix:	n/a	n/a
43	POLR2A	chr6:150208437-150208808	Hela-S3	cervix:	n/a	n/a
44	FOSL1	chr6:150208370-150209044	HCT-116	colon:	n/a	chr6:150208601-150208613 chr6:150208696-150208703 chr6:150208766-150208774 chr6:150208695-150208703 chr6:150208695-150208703 chr6:150208764-150208776 chr6:150208449-150208459
45	POLR2A	chr6:150208350-150212272	Hela-S3	cervix:	n/a	n/a
46	SP1	chr6:150208286-150209033	HCT-116	colon:	n/a	chr6:150208388-150208401
47	JUN	chr6:150208463-150208920	Hela-S3	cervix:	n/a	chr6:150208601-150208613 chr6:150208696-150208703 chr6:150208766-150208774 chr6:150208695-150208703 chr6:150208695-150208703 chr6:150208764-150208776
48	POLR2A	chr6:150208325-150208985	U87	brain:	n/a	n/a
49	STAT3	chr6:150208539-150209004	MCF10A-Er-Src	breast:	n/a	n/a
50	JUND	chr6:150208509-150209005	Hela-S3	cervix:	n/a	chr6:150208601-150208613 chr6:150208696-150208703 chr6:150208766-150208774 chr6:150208693-150208704 chr6:150208695-150208703 chr6:150208695-150208703 chr6:150208764-150208776

No.	Distal block	Cell Line	Cell type
1	chr6:150182126..150185111-chr6:150208101..150209742,2	K562	blood:
2	chr6:150201367..150203467-chr6:150207974..150210289,2	MCF-7	breast:
3	chr6:150182126..150186554-chr6:150208101..150210542,3	K562	blood:
4	chr6:150183161..150188305-chr6:150206346..150214162,9	MCF-7	breast:
5	chr6:150208190..150211087-chr6:150219720..150221224,2	MCF-7	breast:
6	chr6:150182396..150187721-chr6:150207302..150210632,6	MCF-7	breast:
7	chr6:150200712..150203416-chr6:150207860..150210756,3	MCF-7	breast:

Variant related genes	Relation type
RAET1E-AS1	TF binding region
ENSG00000268592	Chromatin interaction
ENSG00000120256	Chromatin interaction
ENSG00000217733	Chromatin interaction

Extended variants
information (count: 65 )
Associated
traits (count: 14 )

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs1334510	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2095376	1.00[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2342767	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2342768	0.83[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs2342769	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2342770	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3823021	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4458704	1.00[CEU][hapmap];0.81[JPT][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4869763	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4869764	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4870116	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6557133	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6925151	0.88[YRI][hapmap]
rs6933882	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6935829	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6939761	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7740145	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7742692	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7742993	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7744821	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7747435	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7747457	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7753544	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7756850	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7757972	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7758020	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7758033	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7763719	0.81[EUR][1000 genomes]
rs7763849	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7764376	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7767588	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7767592	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7768626	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7768665	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7769118	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7771014	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7774787	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9322225	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9322228	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9371215	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9371223	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9371504	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9371505	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9371533	0.92[CEU][hapmap];0.91[CHB][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9371541	0.91[ASN][1000 genomes]
rs9371542	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9371544	0.88[CEU][hapmap];0.84[CHB][hapmap];0.90[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9383577	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9383584	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9383912	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9383913	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9383914	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9383921	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9383940	1.00[CEU][hapmap];0.81[JPT][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9397058	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9397398	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9397420	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9397434	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9397438	0.85[JPT][hapmap]
rs9968871	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9969044	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9986576	0.82[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886764	chr6:150114745-150393683	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv517022	chr6:150145001-150426272	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv886765	chr6:150198491-150288722	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:14)

SNP	Gene	Cis/trans	Tissue	Source
rs7757984	NUP43	Cis_1M	lymphoblastoid	RTeQTL
rs7757984	RAET1G	cis	Esophagus Mucosa	GTEx
rs7757984	RP11-350J20.5	cis	Thyroid	GTEx
rs7757984	RP11-350J20.9	cis	Esophagus Mucosa	GTEx
rs7757984	RP11-350J20.5	cis	lung	GTEx
rs7757984	RP11-350J20.9	cis	lung	GTEx
rs7757984	RP11-350J20.5	cis	Skin Sun Exposed Lower leg	GTEx
rs7757984	RP11-350J20.5	cis	Artery Tibial	GTEx
rs7757984	C6orf72	Cis_1M	lymphoblastoid	RTeQTL
rs7757984	LRP11	cis	Adipose Subcutaneous	GTEx
rs7757984	RAET1E	cis	Nerve Tibial	GTEx
rs7757984	RAET1G	cis	Artery Tibial	GTEx
rs7757984	LRP11	cis	Skin Sun Exposed Lower leg	GTEx
rs7757984	RP11-350J20.9	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150205000-150210400	Enhancers	HMEC	breast
2	chr6:150205600-150216000	Weak transcription	Right Atrium	heart
3	chr6:150205800-150210200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:150205800-150216000	Weak transcription	Stomach Smooth Muscle	stomach
5	chr6:150206000-150208800	Weak transcription	Adipose Nuclei	Adipose
6	chr6:150206000-150216000	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr6:150206600-150211600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr6:150207800-150208800	Enhancers	A549	lung
9	chr6:150207800-150210600	Enhancers	NHDF-Ad	bronchial
10	chr6:150208000-150208800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr6:150208000-150209000	Flanking Active TSS	NHEK	skin
12	chr6:150208000-150210600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:150208000-150210600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr6:150208000-150210800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:150208000-150211800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr6:150208200-150210200	Enhancers	Esophagus	oesophagus
17	chr6:150208200-150210400	Enhancers	Fetal Intestine Small	intestine
18	chr6:150208200-150210400	Enhancers	NHLF	lung
19	chr6:150208200-150210400	Enhancers	Osteobl	bone
20	chr6:150208200-150210600	Enhancers	Muscle Satellite Cultured Cells	--
21	chr6:150208200-150210600	Enhancers	Fetal Intestine Large	intestine
22	chr6:150208400-150209000	Enhancers	NH-A	brain
23	chr6:150208400-150210400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr6:150208400-150211400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr6:150208400-150211600	Weak transcription	Placenta	Placenta
26	chr6:150208400-150212600	Enhancers	Skeletal Muscle Male	skeletal muscle
27	chr6:150208400-150212600	Flanking Active TSS	Hela-S3	cervix
28	chr6:150208600-150208800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr6:150208600-150211400	Enhancers	HSMMtube	muscle

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