Variant report

Variant	rs7794485
Chromosome Location	chr7:100068936-100068937
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr7:100068682-100069068	GM12878	blood:	n/a	n/a
2	POLR2A	chr7:100068850-100069156	GM12878	blood:	n/a	n/a
3	POLR2A	chr7:100067785-100069139	K562	blood:	n/a	n/a
4	POLR2A	chr7:100068878-100069050	K562	blood:	n/a	n/a

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:100065954..100070827-chr7:100162698..100165986,5	K562	blood:
2	chr7:100066903..100068975-chr7:100183632..100186359,3	K562	blood:
3	chr7:100054484..100057296-chr7:100067069..100069392,2	K562	blood:
4	chr7:100067476..100069249-chr7:100098518..100100831,2	MCF-7	breast:
5	chr7:100065519..100069193-chr7:100181232..100183900,3	MCF-7	breast:
6	chr7:100065847..100069259-chr7:100079326..100082103,3	K562	blood:
7	chr7:100068011..100070827-chr7:100164018..100165964,3	K562	blood:
8	chr7:100067039..100069939-chr7:100143624..100146249,2	K562	blood:
9	chr7:100025008..100029373-chr7:100066006..100070271,5	MCF-7	breast:
10	chr7:100068696..100070699-chr7:100288610..100291361,2	MCF-7	breast:
11	chr7:100024700..100032514-chr7:100067180..100083143,31	K562	blood:
12	chr7:100065847..100069421-chr7:100079326..100082103,4	K562	blood:
13	chr7:100022010..100030260-chr7:100068697..100082544,31	K562	blood:

No data

Variant related genes	Relation type
TSC22D4	TF binding region
ENSG00000166924	Chromatin interaction
ENSG00000266372	Chromatin interaction
ENSG00000078487	Chromatin interaction
ENSG00000146834	Chromatin interaction
ENSG00000106336	Chromatin interaction
ENSG00000077454	Chromatin interaction

Extended variants
information (count: 102 )
Associated
traits (count: 59 )

rSNPs within LD-proxies of this variant (count:90)

rs_ID	r²[population]
rs1000215	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.81[EUR][1000 genomes]
rs10085549	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs10241492	1.00[CEU][hapmap]
rs1073	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11559117	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11760536	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.95[TSI][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11761253	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs11761426	0.85[CEU][hapmap]
rs11761624	1.00[ASN][1000 genomes]
rs11761725	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.95[TSI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11761784	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11763414	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs11763511	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11764818	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11765869	1.00[ASW][hapmap];0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.96[MKK][hapmap]
rs11766202	1.00[ASN][1000 genomes]
rs11766752	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11769057	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs11769700	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11769886	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.95[TSI][hapmap]
rs11771241	1.00[CEU][hapmap]
rs11771419	1.00[CEU][hapmap]
rs11772580	1.00[ASN][1000 genomes]
rs11773661	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1962269	0.92[CEU][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2003507	0.81[EUR][1000 genomes]
rs2406253	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2406255	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28490152	1.00[CEU][hapmap];1.00[CHD][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.81[EUR][1000 genomes]
rs28578163	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.80[EUR][1000 genomes]
rs28629346	1.00[ASN][1000 genomes]
rs28660238	0.81[EUR][1000 genomes]
rs2897358	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34989573	0.93[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];0.90[TSI][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35111986	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.95[TSI][hapmap]
rs3900792	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[TSI][hapmap];0.81[EUR][1000 genomes]
rs4074838	0.93[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4385401	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4463351	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4469386	1.00[ASN][1000 genomes]
rs4472444	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4989959	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60257855	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60478351	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60644673	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60844404	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66632384	0.81[EUR][1000 genomes]
rs66648318	1.00[ASN][1000 genomes]
rs66958101	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67040465	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs67163493	0.81[EUR][1000 genomes]
rs67196635	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67239991	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67315960	0.81[EUR][1000 genomes]
rs67471932	0.81[EUR][1000 genomes]
rs67483801	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67885733	1.00[ASN][1000 genomes]
rs68116612	0.81[EUR][1000 genomes]
rs6945952	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs6946768	1.00[ASW][hapmap];1.00[GIH][hapmap];0.93[MKK][hapmap]
rs6948685	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs6948699	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6953107	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6955362	1.00[CEU][hapmap];0.83[CHD][hapmap];1.00[GIH][hapmap];0.95[TSI][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6955367	0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap]
rs6957928	0.81[EUR][1000 genomes]
rs6962151	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6965458	1.00[ASW][hapmap];0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.85[MEX][hapmap];0.96[MKK][hapmap]
rs6970806	0.81[EUR][1000 genomes]
rs6972167	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6974286	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6975514	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6975729	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6978739	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6979335	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6979910	0.85[CEU][hapmap]
rs705866	1.00[ASW][hapmap];0.85[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.96[MKK][hapmap]
rs73161759	0.81[EUR][1000 genomes]
rs73403312	0.81[EUR][1000 genomes]
rs73405353	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7341507	0.85[CEU][hapmap]
rs7783159	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.95[TSI][hapmap];0.81[EUR][1000 genomes]
rs7783550	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap]
rs7787620	0.92[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];0.89[TSI][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7787825	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7792525	0.85[CEU][hapmap]
rs7792959	0.85[CEU][hapmap]
rs7800667	1.00[ASN][1000 genomes]
rs7809801	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7811142	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3350965	chr7:99747460-100146105	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
2	esv1829095	chr7:99814675-100494084	Bivalent Enhancer Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	393 gene(s)	inside rSNPs	diseases
3	nsv831071	chr7:99918025-100113413	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	287 gene(s)	inside rSNPs	diseases
4	nsv888776	chr7:100014711-100198386	Flanking Active TSS Enhancers Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer 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
5	nsv888777	chr7:100014711-100221867	Transcr. at gene 5' and 3' Genic enhancers Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	304 gene(s)	inside rSNPs	diseases
6	nsv888778	chr7:100014711-100236593	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	310 gene(s)	inside rSNPs	diseases
7	nsv888779	chr7:100014711-100313420	Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	321 gene(s)	inside rSNPs	diseases
8	nsv888780	chr7:100032665-100198386	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription 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 miRNA target site	81 gene(s)	inside rSNPs	diseases
9	nsv984550	chr7:100034415-100080060	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
10	nsv527050	chr7:100056166-100125975	Strong transcription Weak transcription Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
11	nsv888781	chr7:100060928-100097895	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
12	nsv888782	chr7:100064719-100236593	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases

mRNA abundance (count:59)

SNP	Gene	Cis/trans	Tissue	Source
rs7794485	STAG3L5P	cis	Muscle Skeletal	GTEx
rs7794485	PILRB	cis	parietal	SCAN
rs7794485	PILRB	cis	Adipose Subcutaneous	GTEx
rs7794485	PILRA	cis	Esophagus Mucosa	GTEx
rs7794485	PILRA	cis	Adipose Subcutaneous	GTEx
rs7794485	PVRIG2P	cis	Nerve Tibial	GTEx
rs7794485	PVRIG	cis	cerebellum	SCAN
rs7794485	PILRB	cis	Whole Blood	GTEx
rs7794485	PILRB	cis	Artery Tibial	GTEx
rs7794485	PILRB	cis	lung	GTEx
rs7794485	PVRIG2P	cis	Adipose Subcutaneous	GTEx
rs7794485	PILRB	cis	Esophagus Mucosa	GTEx
rs7794485	PILRB	cis	Muscle Skeletal	GTEx
rs7794485	STAG3L5P	cis	Heart Left Ventricle	GTEx
rs7794485	PILRB	cis	Artery Aorta	GTEx
rs7794485	ZCWPW1	cis	cerebellum	SCAN
rs7794485	STAG3L5P	cis	Nerve Tibial	GTEx
rs7794485	PILRA	cis	Artery Aorta	GTEx
rs7794485	STAG3L5P	cis	Artery Aorta	GTEx
rs7794485	PILRB	Cis_1M	lymphoblastoid	RTeQTL
rs7794485	PILRB	cis	cerebellum	SCAN
rs7794485	PILRB	cis	Heart Left Ventricle	GTEx
rs7794485	STAG3L5P	cis	Adipose Subcutaneous	GTEx
rs7794485	STAG3L5P	cis	Esophagus Mucosa	GTEx
rs7794485	PILRB	cis	Thyroid	GTEx
rs7794485	PILRA	cis	Stomach	GTEx
rs7794485	PILRA	cis	cerebellum	SCAN
rs7794485	STAG3	Cis_1M	lymphoblastoid	RTeQTL
rs7794485	STAG3L5P	cis	Thyroid	GTEx
rs7794485	PILRA	cis	Skin Sun Exposed Lower leg	GTEx
rs7794485	PVRIG2P	cis	lung	GTEx
rs7794485	PILRA	cis	Artery Tibial	GTEx
rs7794485	PILRA	cis	Muscle Skeletal	GTEx
rs7794485	PILRB	cis	multi-tissue	Pritchard
rs7794485	PILRB	cis	Esophagus Muscularis	GTEx
rs7794485	MEPCE	cis	multi-tissue	Pritchard
rs7794485	GATS	cis	parietal	SCAN
rs7794485	PVRIG2P	cis	Artery Tibial	GTEx
rs7794485	PVRIG2P	cis	Esophagus Muscularis	GTEx
rs7794485	PVRIG2P	cis	Thyroid	GTEx
rs7794485	PILRB	cis	Skin Sun Exposed Lower leg	GTEx
rs7794485	PILRA	cis	Heart Left Ventricle	GTEx
rs7794485	PILRB	cis	Nerve Tibial	GTEx
rs7794485	ZCWPW1	cis	parietal	SCAN
rs7794485	PVRIG2P	cis	Esophagus Mucosa	GTEx
rs7794485	PVRIG	Cis_1M	lymphoblastoid	RTeQTL
rs7794485	STAG3L5P	cis	lung	GTEx
rs7794485	PILRA	cis	Esophagus Muscularis	GTEx
rs7794485	PILRA	cis	Thyroid	GTEx
rs7794485	PILRB	cis	lymphoblastoid	seeQTL
rs7794485	STAG3L5P	cis	Artery Tibial	GTEx
rs7794485	STAG3L5P	cis	Esophagus Muscularis	GTEx
rs7794485	CNPY4	cis	cerebellum	SCAN
rs7794485	MEPCE	cis	lymphoblastoid	seeQTL
rs7794485	PILRA	cis	Nerve Tibial	GTEx
rs7794485	GNB2	cis	parietal	SCAN
rs7794485	PILRA	cis	parietal	SCAN
rs7794485	STAG3L5P	cis	Skin Sun Exposed Lower leg	GTEx
rs7794485	PMS2P1	cis	Thyroid	GTEx

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100048600-100070400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:100048600-100070400	Weak transcription	HSMMtube	muscle
3	chr7:100054200-100069400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr7:100058800-100070400	Weak transcription	Primary hematopoietic stem cells	blood
5	chr7:100061200-100069800	Weak transcription	HMEC	breast
6	chr7:100061400-100070200	Weak transcription	HSMM	muscle
7	chr7:100063200-100069600	Weak transcription	Right Atrium	heart
8	chr7:100063400-100070400	Weak transcription	HUVEC	blood vessel
9	chr7:100063600-100071600	Weak transcription	Fetal Kidney	kidney
10	chr7:100063800-100073000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr7:100063800-100073400	Weak transcription	NH-A	brain
12	chr7:100064000-100073200	Strong transcription	Thymus	Thymus
13	chr7:100064000-100073400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr7:100064200-100069600	Strong transcription	Lung	lung
15	chr7:100064200-100070400	Weak transcription	NHDF-Ad	bronchial
16	chr7:100064200-100070600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr7:100064200-100070800	Weak transcription	Rectal Smooth Muscle	rectum
18	chr7:100064200-100073000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr7:100064400-100069600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr7:100064600-100069200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr7:100064600-100073000	Strong transcription	Dnd41	blood
22	chr7:100065000-100074800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr7:100065400-100070400	Weak transcription	Small Intestine	intestine
24	chr7:100065600-100069600	Weak transcription	NHEK	skin
25	chr7:100065800-100070600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr7:100065800-100075200	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr7:100066000-100070400	Weak transcription	Ovary	ovary
28	chr7:100066200-100073000	Weak transcription	Brain Angular Gyrus	brain
29	chr7:100066400-100069400	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr7:100066400-100070200	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr7:100067000-100069000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr7:100067000-100071600	Strong transcription	NHLF	lung
33	chr7:100067200-100069800	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr7:100067400-100069000	Strong transcription	Primary B cells from peripheral blood	blood
35	chr7:100067400-100069000	Weak transcription	Right Ventricle	heart
36	chr7:100067400-100069400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr7:100067400-100069600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr7:100067400-100069600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr7:100067400-100070200	Weak transcription	Duodenum Mucosa	Duodenum
40	chr7:100067400-100070200	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr7:100067400-100070400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr7:100067400-100070400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr7:100067400-100070600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr7:100067400-100070600	Weak transcription	Liver	Liver
45	chr7:100067400-100070600	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr7:100067400-100070600	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr7:100067400-100070800	Weak transcription	Brain Anterior Caudate	brain
48	chr7:100067400-100073200	Weak transcription	Brain Substantia Nigra	brain
49	chr7:100067400-100073600	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr7:100067400-100074400	Weak transcription	Psoas Muscle	Psoas

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