Variant report

Variant	rs7791995
Chromosome Location	chr7:11055184-11055185
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:11050410..11053088-chr7:11054274..11057224,2	K562	blood:
2	chr7:11012835..11015208-chr7:11055088..11057160,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000106443	Chromatin interaction

Extended variants
information (count: 180 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:166)

rs_ID	r²[population]
rs10234395	0.92[CHB][hapmap];0.81[CHD][hapmap]
rs10236024	1.00[CHB][hapmap];0.95[CHD][hapmap];0.86[JPT][hapmap];0.88[ASN][1000 genomes]
rs10251095	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10251185	1.00[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap]
rs10255688	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs1029583	0.83[CEU][hapmap];0.96[MEX][hapmap]
rs1029584	0.83[CEU][hapmap];0.81[EUR][1000 genomes]
rs1057436	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs10950334	0.95[MEX][hapmap];0.81[EUR][1000 genomes]
rs1154920	0.96[ASN][1000 genomes]
rs1154922	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs11560245	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11762175	0.96[ASN][1000 genomes]
rs11975710	0.96[CEU][hapmap];0.89[GIH][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11978518	1.00[CHB][hapmap];0.85[CHD][hapmap]
rs12112674	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs12699172	0.92[CHB][hapmap]
rs13227933	1.00[CHB][hapmap];0.93[JPT][hapmap];0.86[ASN][1000 genomes]
rs13232272	0.96[CEU][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13236926	0.81[ASN][1000 genomes]
rs13238887	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs13241511	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs1483201	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1483202	0.96[CEU][hapmap];0.89[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1483203	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1483204	0.80[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1483205	0.96[ASN][1000 genomes]
rs1531834	0.92[ASN][1000 genomes]
rs1547945	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1629587	0.96[ASN][1000 genomes]
rs1636753	0.92[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1636754	1.00[ASN][1000 genomes]
rs1636755	0.99[ASN][1000 genomes]
rs1636756	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1636757	1.00[ASN][1000 genomes]
rs1640700	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs1640704	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1640707	0.92[ASN][1000 genomes]
rs1640710	0.99[ASN][1000 genomes]
rs1681281	1.00[ASN][1000 genomes]
rs1681284	0.92[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs1681290	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1681291	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1681298	0.92[ASN][1000 genomes]
rs1681300	0.92[ASN][1000 genomes]
rs1681302	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs1681305	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs1681310	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1681312	0.99[ASN][1000 genomes]
rs17346506	0.95[CEU][hapmap];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs17347241	0.87[CEU][hapmap];0.96[MEX][hapmap];0.88[TSI][hapmap];0.88[EUR][1000 genomes]
rs182594	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1833011	0.86[ASN][1000 genomes]
rs190073	0.89[ASN][1000 genomes]
rs2108111	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs2108114	0.90[ASN][1000 genomes]
rs2110376	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs218968	0.84[CHB][hapmap];0.90[CHD][hapmap];0.93[JPT][hapmap];0.92[ASN][1000 genomes]
rs218975	0.93[ASN][1000 genomes]
rs218980	0.96[ASN][1000 genomes]
rs218981	0.96[ASN][1000 genomes]
rs2190293	0.87[CEU][hapmap];0.91[MEX][hapmap];0.83[EUR][1000 genomes]
rs2190294	0.96[ASN][1000 genomes]
rs2190295	0.96[ASN][1000 genomes]
rs220089	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs220090	0.92[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs220091	1.00[CEU][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs220092	0.97[ASN][1000 genomes]
rs220093	0.97[ASN][1000 genomes]
rs220094	1.00[CEU][hapmap];0.93[GIH][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs220095	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs220096	0.88[EUR][1000 genomes]
rs220097	1.00[CEU][hapmap];0.98[GIH][hapmap];0.96[MEX][hapmap];0.98[TSI][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2214858	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2301959	0.94[EUR][1000 genomes]
rs2353340	1.00[CEU][hapmap];0.93[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2353341	0.96[CEU][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2353342	0.96[CEU][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2353344	0.96[CEU][hapmap]
rs2539823	0.99[ASN][1000 genomes]
rs2625440	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2906543	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2906544	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2906545	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2906546	0.86[ASN][1000 genomes]
rs2906547	0.86[ASN][1000 genomes]
rs2906548	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs2906549	0.83[ASN][1000 genomes]
rs2906550	1.00[CHB][hapmap];0.81[JPT][hapmap];0.86[ASN][1000 genomes]
rs2906551	1.00[CHB][hapmap];0.89[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2906552	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2906553	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2906554	0.84[ASN][1000 genomes]
rs2906555	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2906556	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2906557	0.81[ASN][1000 genomes]
rs2906558	0.91[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2906559	0.86[ASN][1000 genomes]
rs2906560	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2906561	0.86[ASN][1000 genomes]
rs2906562	0.86[ASN][1000 genomes]
rs2906563	0.86[ASN][1000 genomes]
rs2906564	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2906565	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[TSI][hapmap];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2906566	0.87[ASN][1000 genomes]
rs2995878	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2995879	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2995880	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2995881	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2995884	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2995886	0.82[ASN][1000 genomes]
rs2995898	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2995901	0.86[ASN][1000 genomes]
rs2995902	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2995903	1.00[CHB][hapmap];0.85[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs34166672	0.87[EUR][1000 genomes]
rs34295894	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34665460	0.83[EUR][1000 genomes]
rs35507980	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35580506	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35594158	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35648039	0.82[EUR][1000 genomes]
rs3801435	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3801437	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs3801441	0.95[CEU][hapmap];0.91[GIH][hapmap];0.87[MEX][hapmap];0.95[TSI][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs3801444	0.96[CEU][hapmap];0.91[GIH][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3801449	0.86[CEU][hapmap];0.87[EUR][1000 genomes]
rs3801450	0.87[CEU][hapmap];0.95[MEX][hapmap];0.86[TSI][hapmap];0.88[EUR][1000 genomes]
rs3801451	0.84[EUR][1000 genomes]
rs3801453	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs3823875	1.00[CHB][hapmap];0.86[JPT][hapmap];0.93[ASN][1000 genomes]
rs4314555	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs4342485	1.00[ASN][1000 genomes]
rs4370426	0.88[EUR][1000 genomes]
rs4534044	0.86[ASN][1000 genomes]
rs4644135	1.00[CHB][hapmap];0.81[CHD][hapmap]
rs4719258	1.00[CHB][hapmap];0.85[CHD][hapmap]
rs4719260	0.84[CHB][hapmap]
rs4720938	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs4720946	0.92[CHB][hapmap];0.81[CHD][hapmap]
rs62440480	0.94[EUR][1000 genomes]
rs6460785	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6460789	0.92[CHB][hapmap]
rs6943379	0.97[ASN][1000 genomes]
rs6944741	0.92[CHB][hapmap]
rs6954805	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs6957940	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6968425	0.87[ASN][1000 genomes]
rs6973228	1.00[ASN][1000 genomes]
rs7781258	0.86[ASN][1000 genomes]
rs7782589	0.96[CEU][hapmap];0.89[GIH][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7785008	1.00[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs7786922	0.92[CHB][hapmap];0.80[CHD][hapmap]
rs7789963	0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7790383	1.00[CHB][hapmap];0.85[CHD][hapmap]
rs7790448	0.84[CHB][hapmap];1.00[JPT][hapmap]
rs7794514	0.84[CHB][hapmap]
rs7798427	0.92[CHB][hapmap];0.85[CHD][hapmap]
rs7803348	0.82[EUR][1000 genomes]
rs7806840	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7809178	0.84[CHB][hapmap];1.00[JPT][hapmap]
rs8180695	0.95[ASN][1000 genomes]
rs922901	0.82[CHB][hapmap];0.93[JPT][hapmap];0.89[ASN][1000 genomes]
rs9639071	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9768601	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9986755	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1067780	chr7:10649696-11329787	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv491695	chr7:10649696-11329787	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv1019888	chr7:10712858-11496785	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv1029836	chr7:10713523-11492751	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers 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 target site	31 gene(s)	inside rSNPs	diseases
5	nsv538730	chr7:10713523-11492751	Weak transcription Strong transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
6	nsv532092	chr7:10731350-11414759	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
7	nsv887600	chr7:10807685-11090546	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
8	nsv1024171	chr7:10810444-11559156	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
9	nsv949387	chr7:10815994-11281536	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
10	nsv1029882	chr7:10872162-11371145	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
11	nsv817291	chr7:10875417-11562683	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
12	nsv1031498	chr7:10882696-11110412	Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
13	nsv1030035	chr7:11027819-11256089	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
14	nsv606194	chr7:11042905-11144078	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7791995	GLCCI1	cis	cerebellum	SCAN

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:11014600-11092000	Weak transcription	Colonic Mucosa	Colon
2	chr7:11014800-11075200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr7:11014800-11117400	Weak transcription	HSMMtube	muscle
4	chr7:11015000-11064000	Weak transcription	Colon Smooth Muscle	Colon
5	chr7:11015200-11108200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr7:11016800-11057200	Weak transcription	Fetal Brain Male	brain
7	chr7:11017200-11076000	Weak transcription	HUVEC	blood vessel
8	chr7:11018600-11063800	Weak transcription	Brain Angular Gyrus	brain
9	chr7:11022800-11071000	Weak transcription	Right Ventricle	heart
10	chr7:11023200-11076200	Weak transcription	NH-A	brain
11	chr7:11031600-11103800	Weak transcription	Brain Cingulate Gyrus	brain
12	chr7:11034800-11064200	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr7:11035400-11064000	Weak transcription	Brain Germinal Matrix	brain
14	chr7:11035800-11057200	Weak transcription	Spleen	Spleen
15	chr7:11035800-11063000	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr7:11035800-11063800	Weak transcription	Brain Hippocampus Middle	brain
17	chr7:11035800-11076000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr7:11035800-11092600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr7:11035800-11113000	Weak transcription	Esophagus	oesophagus
20	chr7:11035800-11113200	Weak transcription	Lung	lung
21	chr7:11035800-11123000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr7:11036000-11101600	Weak transcription	Placenta	Placenta
23	chr7:11036600-11063600	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr7:11036600-11100800	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr7:11038800-11063800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr7:11039000-11066800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr7:11039000-11090600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
28	chr7:11039000-11108800	Weak transcription	Psoas Muscle	Psoas
29	chr7:11039400-11063600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr7:11039600-11063800	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr7:11046000-11128600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr7:11046200-11175000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr7:11046400-11062600	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr7:11046600-11063600	Weak transcription	Fetal Brain Female	brain
35	chr7:11046600-11081200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr7:11046600-11103400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr7:11046600-11122600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr7:11046600-11167800	Weak transcription	Thymus	Thymus
39	chr7:11046800-11059600	Weak transcription	Fetal Intestine Small	intestine
40	chr7:11046800-11059600	Weak transcription	Fetal Stomach	stomach
41	chr7:11048200-11071600	Weak transcription	Gastric	stomach
42	chr7:11048200-11098600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr7:11048200-11113400	Weak transcription	Aorta	Aorta
44	chr7:11049400-11063800	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr7:11049800-11063800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr7:11050800-11064000	Weak transcription	NHEK	skin
47	chr7:11051000-11076000	Weak transcription	HMEC	breast
48	chr7:11051600-11056800	Strong transcription	Dnd41	blood
49	chr7:11052200-11063600	Weak transcription	Brain Anterior Caudate	brain
50	chr7:11052800-11055600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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