Variant report

Variant	rs7958662
Chromosome Location	chr12:1401140-1401141
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 128 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs1005394	0.80[CEU][hapmap];0.88[CHB][hapmap]
rs1012719	0.85[CEU][hapmap];0.80[AMR][1000 genomes]
rs10161285	0.94[CHB][hapmap]
rs1017019	0.81[ASN][1000 genomes]
rs10848452	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10848456	1.00[CHB][hapmap];0.82[JPT][hapmap]
rs10848458	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11061677	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11061679	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11061682	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11061691	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11061698	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11061699	0.88[CHB][hapmap];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11061702	0.88[CHB][hapmap];0.82[JPT][hapmap]
rs11061703	0.88[CHB][hapmap]
rs11061707	0.82[CEU][hapmap];0.89[CHB][hapmap]
rs11061712	0.85[CEU][hapmap];0.88[CHB][hapmap];0.81[EUR][1000 genomes]
rs11061714	0.81[CEU][hapmap];0.88[CHB][hapmap];0.81[EUR][1000 genomes]
rs11061736	0.82[CHB][hapmap]
rs11061737	0.84[CEU][hapmap];0.88[CHB][hapmap]
rs11609402	0.81[ASN][1000 genomes]
rs11835033	0.81[ASN][1000 genomes]
rs11836372	0.85[CEU][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11837688	0.81[CEU][hapmap];0.88[CHB][hapmap]
rs12298813	0.88[CHB][hapmap]
rs12302807	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12306160	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12306260	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12315865	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12317763	0.81[CEU][hapmap]
rs12423105	0.84[CEU][hapmap];0.88[CHB][hapmap]
rs12426509	0.94[CHB][hapmap];0.81[ASN][1000 genomes]
rs1419965	0.81[EUR][1000 genomes]
rs1544425	0.81[CEU][hapmap];0.94[CHB][hapmap];0.81[ASN][1000 genomes]
rs16928347	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17223448	0.88[CHB][hapmap]
rs17800876	0.81[CEU][hapmap];0.94[CHB][hapmap]
rs2051843	0.81[EUR][1000 genomes]
rs2189788	0.88[CHB][hapmap]
rs2286031	0.88[CHB][hapmap]
rs2286037	0.94[CHB][hapmap];0.85[ASN][1000 genomes]
rs2906109	0.83[CHB][hapmap]
rs2968874	0.83[CHB][hapmap]
rs34929071	0.81[EUR][1000 genomes]
rs4766249	0.84[ASN][1000 genomes]
rs56742512	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57027936	0.85[ASN][1000 genomes]
rs57125493	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs57707051	0.81[EUR][1000 genomes]
rs58159804	0.81[ASN][1000 genomes]
rs58545225	0.85[ASN][1000 genomes]
rs60222319	0.83[EUR][1000 genomes]
rs61009778	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61911976	0.84[ASN][1000 genomes]
rs61911977	0.84[ASN][1000 genomes]
rs61911978	0.84[ASN][1000 genomes]
rs61911983	0.85[ASN][1000 genomes]
rs61911984	0.85[ASN][1000 genomes]
rs61912026	0.85[ASN][1000 genomes]
rs61913073	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs61913075	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61913099	0.82[AMR][1000 genomes]
rs6489270	0.88[CHB][hapmap]
rs6489273	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6489274	0.83[ASN][1000 genomes]
rs6489276	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6489277	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6489282	0.84[CEU][hapmap];0.88[CHB][hapmap]
rs7137058	0.88[CHB][hapmap]
rs7300575	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7300981	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7303850	0.88[CHB][hapmap]
rs7306130	1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7311231	0.81[EUR][1000 genomes]
rs7313311	0.81[CEU][hapmap];0.88[CHB][hapmap]
rs766956	0.84[CEU][hapmap];0.88[CHB][hapmap]
rs7954213	0.89[CHB][hapmap]
rs7956588	0.85[CEU][hapmap]
rs7962697	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7963602	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7967934	0.92[CEU][hapmap];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7968223	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7968583	0.84[CEU][hapmap];0.88[CHB][hapmap]
rs7968772	0.80[AMR][1000 genomes]
rs7971585	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7971670	0.94[CHB][hapmap]
rs7972290	0.92[CEU][hapmap];0.88[CHB][hapmap];0.86[EUR][1000 genomes]
rs7973820	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7975854	0.96[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7976337	0.81[ASN][1000 genomes]
rs7978540	0.84[CEU][hapmap];0.88[CHB][hapmap]
rs7978898	0.84[CEU][hapmap];0.88[CHB][hapmap];0.81[EUR][1000 genomes]
rs7980065	0.94[CHB][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs7980582	0.81[ASN][1000 genomes]
rs9943818	0.93[CEU][hapmap];0.94[CHB][hapmap];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9943854	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:32 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898576	chr12:813411-1553450	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv948760	chr12:863833-1542875	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv1052589	chr12:910460-1421493	ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv1045278	chr12:920251-1697030	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
5	nsv529398	chr12:941915-1741311	Weak transcription Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
6	nsv468960	chr12:975276-1455106	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv556941	chr12:975276-1455106	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
8	nsv1044329	chr12:985144-1403020	Genic enhancers Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats 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	33 gene(s)	inside rSNPs	diseases
9	nsv541340	chr12:985144-1403020	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
10	nsv470256	chr12:998365-1438761	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
11	nsv898579	chr12:1013176-1510505	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
12	nsv898580	chr12:1024688-1569097	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
13	nsv1036488	chr12:1041097-1445923	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
14	nsv1037825	chr12:1045734-1432940	Bivalent/Poised TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
15	nsv541342	chr12:1045734-1432940	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
16	esv2762958	chr12:1049279-1554962	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
17	nsv1052559	chr12:1077964-1588543	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
18	nsv898581	chr12:1084783-1527359	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
19	nsv1046134	chr12:1153489-1675223	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
20	nsv541344	chr12:1153489-1675223	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
21	nsv1042863	chr12:1163817-1902302	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer 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	46 gene(s)	inside rSNPs	diseases
22	nsv541345	chr12:1163817-1902302	Strong transcription Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
23	nsv1039826	chr12:1259831-1483326	Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
24	nsv930996	chr12:1270113-1473328	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
25	nsv1050361	chr12:1274052-1541558	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
26	nsv898582	chr12:1286841-1416592	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
27	nsv556944	chr12:1308553-1569097	Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
28	nsv898583	chr12:1314430-1507616	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
29	nsv470257	chr12:1314430-1514021	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
30	nsv1054178	chr12:1372157-1682699	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
31	nsv541347	chr12:1372157-1682699	Bivalent Enhancer Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
32	nsv1035935	chr12:1400974-1608625	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:93 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1334200-1425000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:1341800-1420000	Weak transcription	Esophagus	oesophagus
3	chr12:1364800-1408600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr12:1366600-1418000	Weak transcription	Lung	lung
5	chr12:1369400-1427600	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr12:1373600-1402600	Weak transcription	Hela-S3	cervix
7	chr12:1373800-1410400	Weak transcription	Fetal Intestine Small	intestine
8	chr12:1374200-1404200	Weak transcription	Left Ventricle	heart
9	chr12:1374200-1423200	Weak transcription	NHEK	skin
10	chr12:1375200-1419800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr12:1375400-1404200	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr12:1387400-1453400	Weak transcription	Thymus	Thymus
13	chr12:1387600-1404600	Weak transcription	Fetal Heart	heart
14	chr12:1387600-1441400	Weak transcription	HepG2	liver
15	chr12:1391200-1434000	Weak transcription	A549	lung
16	chr12:1391600-1406000	Weak transcription	Osteobl	bone
17	chr12:1391600-1427800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr12:1391800-1421600	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr12:1392200-1409600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr12:1392200-1413200	Weak transcription	K562	blood
21	chr12:1392400-1404000	Weak transcription	Brain Anterior Caudate	brain
22	chr12:1392400-1405400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr12:1392400-1406600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr12:1392400-1411200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:1392400-1414200	Weak transcription	Psoas Muscle	Psoas
26	chr12:1392400-1414600	Weak transcription	Brain Hippocampus Middle	brain
27	chr12:1392400-1422200	Weak transcription	Ovary	ovary
28	chr12:1392600-1403600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr12:1392600-1415000	Weak transcription	HSMMtube	muscle
30	chr12:1392800-1415400	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr12:1393000-1413400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr12:1393200-1427400	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr12:1394200-1401600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr12:1394200-1401800	Weak transcription	Fetal Muscle Trunk	muscle
35	chr12:1394400-1402800	Weak transcription	Dnd41	blood
36	chr12:1395200-1428000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr12:1396200-1404200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr12:1396800-1408600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr12:1397000-1409200	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr12:1397400-1406000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr12:1397600-1408600	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr12:1398000-1403400	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr12:1398800-1401200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:1398800-1401200	Strong transcription	Primary T cells from cord blood	blood
45	chr12:1398800-1401200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr12:1399000-1401200	Strong transcription	Primary T helper cells PMA-I stimulated	--
47	chr12:1399000-1401200	Strong transcription	Primary T helper cells fromperipheralblood	blood
48	chr12:1399000-1401200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr12:1399000-1401200	Strong transcription	Liver	Liver
50	chr12:1399000-1427600	Weak transcription	Brain Angular Gyrus	brain

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