Variant report

Variant	rs1727140
Chromosome Location	chr7:99815399-99815400
allele	A/T
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	NFATC1	chr7:99814929-99815519	GM12878	blood:	n/a	n/a
2	CTCF	chr7:99815280-99815430	SK-N-SH_RA	brain:	n/a	n/a
3	POLR2A	chr7:99814494-99815878	GM12891	blood:	n/a	n/a
4	POLR2A	chr7:99815173-99815472	GM12878	blood:	n/a	n/a
5	CTCF	chr7:99814615-99816089	K562	blood:	n/a	chr7:99814948-99814961 chr7:99814896-99814914 chr7:99814946-99814964 chr7:99814902-99814911
6	CTCF	chr7:99815394-99815886	HUVEC	blood vessel:	n/a	n/a
7	TCF3	chr7:99814812-99815849	GM12878	blood:	n/a	n/a
8	POLR2A	chr7:99815114-99815585	GM12891	blood:	n/a	n/a
9	POLR2A	chr7:99814334-99815941	GM12878	blood:	n/a	n/a
10	ATF3	chr7:99815130-99815443	GM12878	blood:	n/a	n/a
11	POLR2A	chr7:99814518-99815862	GM12891	blood:	n/a	n/a
12	CTCF	chr7:99815315-99815937	K562	blood:	n/a	n/a
13	TBL1XR1	chr7:99815342-99815476	GM12878	blood:	n/a	n/a
14	POLR2A	chr7:99814584-99815942	GM12891	blood:	n/a	n/a
15	POU2F2	chr7:99814781-99815840	GM12878	blood:	n/a	n/a
16	POLR2A	chr7:99814628-99815852	GM12891	blood:	n/a	n/a
17	BCL11A	chr7:99814744-99815856	GM12878	blood:	n/a	n/a
18	POU2F2	chr7:99814509-99815886	GM12878	blood:	n/a	n/a
19	SPI1	chr7:99815360-99815622	K562	blood:	n/a	n/a
20	SPI1	chr7:99815346-99815593	GM12878	blood:	n/a	n/a
21	JUND	chr7:99815386-99815835	HepG2	liver:	n/a	n/a
22	CTCF	chr7:99815280-99815430	GM12871	blood:	n/a	n/a
23	IRF1	chr7:99815386-99815535	K562	blood:	n/a	n/a
24	USF1	chr7:99815100-99815482	GM12878	blood:	n/a	n/a
25	POLR2A	chr7:99815250-99815932	PANC-1	pancreas:	n/a	n/a
26	CEBPB	chr7:99815339-99815644	GM12878	blood:	n/a	n/a
27	USF1	chr7:99815175-99815953	A549	lung:	n/a	n/a
28	POLR2A	chr7:99814548-99815890	Hela-S3	cervix:	n/a	n/a
29	SP1	chr7:99814755-99815853	GM12878	blood:	n/a	n/a
30	USF1	chr7:99814803-99815865	A549	lung:	n/a	n/a
31	ZEB1	chr7:99814866-99815520	GM12878	blood:	n/a	n/a
32	HEY1	chr7:99815314-99815771	K562	blood:	n/a	n/a
33	CEBPB	chr7:99814679-99815995	GM12878	blood:	n/a	n/a
34	PAX5	chr7:99814634-99815913	GM12878	blood:	n/a	chr7:99815031-99815050
35	CTCF	chr7:99814676-99815514	A549	lung:	n/a	chr7:99814948-99814961 chr7:99814896-99814914 chr7:99814946-99814964 chr7:99814902-99814911
36	IRF4	chr7:99814631-99815997	GM12878	blood:	n/a	n/a
37	NFATC1	chr7:99815084-99815524	GM12878	blood:	n/a	n/a
38	RUNX3	chr7:99814874-99815509	GM12878	blood:	n/a	n/a
39	MTA3	chr7:99814866-99815532	GM12878	blood:	n/a	n/a
40	TCF12	chr7:99815273-99815851	GM12878	blood:	n/a	n/a
41	POLR2A	chr7:99814466-99815887	GM12892	blood:	n/a	n/a
42	POLR2A	chr7:99814353-99815900	GM12892	blood:	n/a	n/a
43	EP300	chr7:99815190-99815839	GM12878	blood:	n/a	n/a
44	EP300	chr7:99815066-99815526	GM12878	blood:	n/a	n/a
45	SPI1	chr7:99815100-99815903	GM12878	blood:	n/a	n/a
46	FOXM1	chr7:99814626-99815853	GM12878	blood:	n/a	n/a
47	CUX1	chr7:99815211-99815454	GM12878	blood:	n/a	n/a
48	TRIM28	chr7:99814618-99815401	K562	blood:	n/a	n/a
49	USF1	chr7:99815096-99815488	K562	blood:	n/a	n/a
50	MTA3	chr7:99815076-99815503	GM12878	blood:	n/a	n/a

Variant related genes	Relation type
PVRIG	TF binding region
ENSG00000239521	TF binding region

Extended variants
information (count: 90 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10252884	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1043915	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1052482	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1061230	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10953295	0.87[CHB][hapmap]
rs1138417	0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11764176	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11767968	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11771139	0.83[CEU][hapmap]
rs12666107	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12666425	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12705073	0.86[CHB][hapmap]
rs13230744	1.00[CEU][hapmap];0.96[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1617502	0.87[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1618851	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1623264	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1624099	0.86[CHB][hapmap]
rs1628077	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1636975	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1636988	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1637001	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1727122	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1727123	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1727124	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1727125	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1727128	0.91[CHB][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs1727130	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1727132	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1727133	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];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1727134	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1727138	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];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1727142	0.97[EUR][1000 genomes]
rs1880949	0.83[CEU][hapmap]
rs2005763	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2141160	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2246713	0.87[CHB][hapmap]
rs2257213	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2272344	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2272345	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2405442	0.95[CHB][hapmap];0.91[JPT][hapmap]
rs2528900	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2906645	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2906646	0.86[CHB][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs2950517	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2950518	0.86[CHB][hapmap]
rs2950520	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34919929	0.83[CHB][hapmap];0.91[JPT][hapmap]
rs35146811	0.83[CEU][hapmap]
rs3735241	0.86[CHB][hapmap];1.00[YRI][hapmap]
rs3735242	0.86[CHB][hapmap]
rs3779045	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3779046	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3823642	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4729579	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55796551	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57966707	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6465764	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6465765	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6465766	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6948729	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6960458	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs705867	0.86[CHB][hapmap]
rs7788301	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7794170	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs7811662	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs858505	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs858506	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs858507	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs858508	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs858509	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs858510	0.81[AFR][1000 genomes]
rs858511	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs858512	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs858513	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs858514	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs863450	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs866500	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs941287	0.86[CHB][hapmap];1.00[YRI][hapmap];0.82[AFR][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	nsv534298	chr7:99478011-99886076	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1132 gene(s)	inside rSNPs	diseases
2	esv1798486	chr7:99689883-99930879	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1085 gene(s)	inside rSNPs	diseases
3	esv1833059	chr7:99689883-99930879	Flanking Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1085 gene(s)	inside rSNPs	diseases
4	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
5	nsv427794	chr7:99750981-99960900	Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
6	nsv428180	chr7:99750981-99960900	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
7	nsv8182	chr7:99799816-99879781	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv888774	chr7:99807265-99951315	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
9	esv16057	chr7:99809377-99937347	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
10	esv3379367	chr7:99811760-99938687	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
11	esv3379649	chr7:99812207-99939196	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
12	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

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs1727140	PVRIG	Cis_1M	lymphoblastoid	RTeQTL
rs1727140	GATS	cis	multi-tissue	Pritchard

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99790000-99817000	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr7:99796800-99816800	Weak transcription	Brain Germinal Matrix	brain
3	chr7:99796800-99817000	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr7:99799000-99816600	Weak transcription	Fetal Brain Female	brain
5	chr7:99801400-99826000	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr7:99803000-99816800	Weak transcription	Brain Angular Gyrus	brain
7	chr7:99805200-99818400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr7:99806800-99819000	Weak transcription	Fetal Lung	lung
9	chr7:99807200-99828400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr7:99807200-99847000	Weak transcription	Fetal Kidney	kidney
11	chr7:99807600-99818400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr7:99809000-99817600	Weak transcription	Small Intestine	intestine
13	chr7:99809200-99817600	Weak transcription	Colonic Mucosa	Colon
14	chr7:99809200-99834800	Weak transcription	HSMMtube	muscle
15	chr7:99809400-99817600	Weak transcription	Spleen	Spleen
16	chr7:99809400-99818200	Weak transcription	Primary hematopoietic stem cells	blood
17	chr7:99809600-99816800	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr7:99809600-99817600	Weak transcription	Dnd41	blood
19	chr7:99809600-99818600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr7:99810600-99864000	Weak transcription	Right Atrium	heart
21	chr7:99810800-99816800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr7:99811200-99818200	Weak transcription	Adipose Nuclei	Adipose
23	chr7:99811400-99817200	Weak transcription	Fetal Intestine Large	intestine
24	chr7:99811400-99817600	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr7:99811400-99828600	Weak transcription	HepG2	liver
26	chr7:99811600-99816800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr7:99811600-99819000	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr7:99811600-99823800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr7:99811600-99834800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr7:99812000-99817600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr7:99812200-99818800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr7:99812200-99819000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr7:99812200-99823800	Weak transcription	Stomach Mucosa	stomach
34	chr7:99812400-99839600	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr7:99812800-99817600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr7:99813000-99815400	Enhancers	Fetal Muscle Leg	muscle
37	chr7:99813200-99815400	Enhancers	Brain Hippocampus Middle	brain
38	chr7:99813600-99815600	Enhancers	Fetal Muscle Trunk	muscle
39	chr7:99813800-99816800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr7:99813800-99816800	Weak transcription	Brain Anterior Caudate	brain
41	chr7:99813800-99816800	Weak transcription	Brain Cingulate Gyrus	brain
42	chr7:99813800-99817000	Weak transcription	Lung	lung
43	chr7:99813800-99817400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr7:99813800-99818400	Weak transcription	Right Ventricle	heart
45	chr7:99813800-99825000	Weak transcription	Psoas Muscle	Psoas
46	chr7:99813800-99829400	Weak transcription	Colon Smooth Muscle	Colon
47	chr7:99813800-99838800	Weak transcription	Fetal Brain Male	brain
48	chr7:99813800-99841200	Weak transcription	Left Ventricle	heart
49	chr7:99813800-99846800	Weak transcription	Ovary	ovary
50	chr7:99814000-99816800	Weak transcription	Brain Substantia Nigra	brain

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