Variant report

Variant	rs7968583
Chromosome Location	chr12:1509621-1509622
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:1509342..1511317-chr12:1517042..1518817,2	K562	blood:
2	chr12:1509342..1510930-chr12:1517317..1520243,2	K562	blood:

Variant related genes	Relation type
ENSG00000082805	Chromatin interaction

Extended variants
information (count: 138 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:113)

rs_ID	r²[population]
rs1005394	1.00[CHB][hapmap];0.80[CHD][hapmap];0.87[ASN][1000 genomes]
rs1012719	0.93[ASN][1000 genomes]
rs10161285	0.82[CHB][hapmap]
rs10773938	0.84[CEU][hapmap];0.88[CHB][hapmap]
rs10773941	0.84[CEU][hapmap];0.88[CHB][hapmap];0.83[CHD][hapmap]
rs10848456	0.85[CEU][hapmap];0.89[CHB][hapmap]
rs10848458	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10848466	0.88[CEU][hapmap];0.88[CHB][hapmap];0.84[JPT][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10848468	0.84[CEU][hapmap];0.88[CHB][hapmap]
rs11061677	0.84[CEU][hapmap];0.88[CHB][hapmap];0.81[GIH][hapmap]
rs11061679	0.87[CEU][hapmap];0.88[CHB][hapmap];0.81[GIH][hapmap]
rs11061682	0.84[CEU][hapmap];0.89[CHB][hapmap]
rs11061691	0.84[CEU][hapmap];0.89[CHB][hapmap];0.82[ASN][1000 genomes]
rs11061698	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11061705	0.87[ASN][1000 genomes]
rs11061707	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs11061712	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11061714	0.96[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.98[TSI][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11061721	0.84[CEU][hapmap];0.88[CHB][hapmap];0.83[CHD][hapmap]
rs11061724	0.84[CEU][hapmap];0.88[CHB][hapmap];0.83[CHD][hapmap]
rs11061729	0.84[CEU][hapmap];0.88[CHB][hapmap]
rs11061730	0.82[CEU][hapmap]
rs11061731	0.83[CEU][hapmap];0.86[CHB][hapmap]
rs11061732	0.84[CEU][hapmap];0.88[CHB][hapmap]
rs11061733	0.84[CEU][hapmap];0.88[CHB][hapmap]
rs11061734	0.84[CEU][hapmap];0.88[CHB][hapmap]
rs11061735	0.84[CEU][hapmap];0.88[CHB][hapmap]
rs11061736	0.94[CHB][hapmap]
rs11061737	0.90[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];0.98[TSI][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11061741	0.88[CHB][hapmap]
rs11061743	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11613252	0.88[CHB][hapmap];0.83[CHD][hapmap]
rs11831980	0.87[CEU][hapmap]
rs11836372	0.82[CHB][hapmap]
rs11837688	1.00[CHB][hapmap];0.80[CHD][hapmap];0.87[ASN][1000 genomes]
rs12298813	0.88[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.91[TSI][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12301879	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12301937	0.88[CHB][hapmap];0.83[CHD][hapmap]
rs12305871	0.88[CHB][hapmap]
rs12306160	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12307046	0.88[CHB][hapmap];0.83[CHD][hapmap]
rs12308521	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12312647	0.86[CHB][hapmap]
rs12314672	0.83[CEU][hapmap];0.87[CHB][hapmap]
rs12316687	0.88[CHB][hapmap];0.82[CHD][hapmap]
rs12317763	0.82[CHB][hapmap]
rs12320293	0.88[CEU][hapmap];0.82[CHB][hapmap];0.87[CHD][hapmap];0.83[GIH][hapmap];0.84[JPT][hapmap];0.85[MEX][hapmap];0.81[TSI][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12320911	0.93[ASN][1000 genomes]
rs12321803	0.88[CHB][hapmap];0.82[CHD][hapmap]
rs12423105	1.00[CHB][hapmap];0.85[CHD][hapmap];0.93[ASN][1000 genomes]
rs12425175	0.84[CEU][hapmap];0.88[CHB][hapmap];0.82[CHD][hapmap]
rs12426509	0.82[CHB][hapmap]
rs1362265	0.88[CHB][hapmap];0.83[CHD][hapmap]
rs1362266	0.82[CHB][hapmap]
rs1419965	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1476908	0.82[CHB][hapmap]
rs1544425	0.82[CHB][hapmap]
rs1548805	0.88[CHB][hapmap]
rs1548806	0.84[CEU][hapmap];0.88[CHB][hapmap];0.83[CHD][hapmap]
rs16928347	0.88[CEU][hapmap];0.84[CHB][hapmap];0.82[TSI][hapmap];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs16928381	0.84[CEU][hapmap];0.88[CHB][hapmap];0.83[CHD][hapmap]
rs16928383	0.87[CEU][hapmap];0.88[CHB][hapmap];0.83[JPT][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs16928393	0.84[CEU][hapmap];0.88[CHB][hapmap]
rs17800876	0.82[CHB][hapmap]
rs2051843	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2051844	0.88[CHB][hapmap]
rs2052185	0.86[CEU][hapmap];0.88[CHB][hapmap]
rs2286031	0.80[CEU][hapmap];0.81[GIH][hapmap]
rs2286037	0.82[CHB][hapmap]
rs34929071	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35579512	0.87[ASN][1000 genomes]
rs41369952	0.88[CHB][hapmap]
rs57707051	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58639324	0.93[ASN][1000 genomes]
rs59141976	0.93[ASN][1000 genomes]
rs61913073	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61913097	0.87[ASN][1000 genomes]
rs61913099	0.93[ASN][1000 genomes]
rs61913128	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6489277	0.84[CEU][hapmap];0.89[CHB][hapmap];0.81[GIH][hapmap]
rs6489282	1.00[CHB][hapmap];0.84[CHD][hapmap];0.93[ASN][1000 genomes]
rs6489284	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7136329	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7300575	0.88[CEU][hapmap];0.84[CHB][hapmap];0.85[GIH][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7300981	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73038635	0.87[ASN][1000 genomes]
rs73038647	0.87[ASN][1000 genomes]
rs7306130	0.84[CEU][hapmap];0.84[CHB][hapmap];0.82[GIH][hapmap]
rs7311231	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7313311	1.00[CHB][hapmap];0.87[ASN][1000 genomes]
rs7488294	0.84[JPT][hapmap]
rs766956	1.00[CHB][hapmap];0.85[CHD][hapmap];0.93[ASN][1000 genomes]
rs768157	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7954162	0.93[ASN][1000 genomes]
rs7956588	0.87[ASN][1000 genomes]
rs7956798	0.87[ASN][1000 genomes]
rs7958662	0.84[CEU][hapmap];0.88[CHB][hapmap]
rs7963546	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7963602	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7967934	0.83[CEU][hapmap]
rs7968223	0.82[ASN][1000 genomes]
rs7968772	0.89[ASN][1000 genomes]
rs7969569	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7971670	0.82[CHB][hapmap]
rs7972088	0.87[ASN][1000 genomes]
rs7972290	0.84[CEU][hapmap];1.00[CHB][hapmap];0.87[CHD][hapmap];0.88[ASN][1000 genomes]
rs7973734	0.88[CEU][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7975854	0.88[CEU][hapmap];0.84[CHB][hapmap];0.83[GIH][hapmap];0.83[TSI][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7978540	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7978898	0.91[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.91[MKK][hapmap];0.95[TSI][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7980065	0.81[CHB][hapmap];0.81[GIH][hapmap];0.80[MEX][hapmap]
rs956408	0.88[CHB][hapmap]
rs9943818	0.84[CEU][hapmap];0.84[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:25 , 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	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	nsv1039946	chr12:1429190-1548852	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
21	nsv1044918	chr12:1432740-1584649	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
22	nsv541348	chr12:1432740-1584649	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
23	nsv556949	chr12:1437726-1514021	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
24	nsv1046515	chr12:1440896-1588543	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
25	nsv1039488	chr12:1486636-1567275	Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Active TSS Flanking 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:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1478400-1520400	Weak transcription	Pancreas	Pancrea
2	chr12:1481400-1520000	Weak transcription	Thymus	Thymus
3	chr12:1486200-1518400	Weak transcription	Primary B cells from peripheral blood	blood
4	chr12:1486800-1530400	Weak transcription	Fetal Lung	lung
5	chr12:1489800-1510800	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr12:1489800-1517600	Weak transcription	Duodenum Mucosa	Duodenum
7	chr12:1489800-1517800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr12:1492000-1512200	Weak transcription	Fetal Heart	heart
9	chr12:1492400-1531200	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr12:1493200-1517000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr12:1494400-1513800	Weak transcription	Liver	Liver
12	chr12:1498400-1529800	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr12:1500600-1518200	Weak transcription	Primary B cells from cord blood	blood
14	chr12:1500800-1517800	Weak transcription	HSMMtube	muscle
15	chr12:1500800-1518200	Weak transcription	HSMM	muscle
16	chr12:1500800-1527200	Weak transcription	Rectal Smooth Muscle	rectum
17	chr12:1500800-1528800	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr12:1501000-1517600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr12:1501000-1517800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr12:1501000-1517800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr12:1501000-1517800	Weak transcription	Fetal Muscle Leg	muscle
22	chr12:1501000-1529800	Weak transcription	Gastric	stomach
23	chr12:1501200-1517600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr12:1501200-1517800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr12:1501200-1519600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr12:1501200-1520000	Weak transcription	Fetal Stomach	stomach
27	chr12:1501200-1530400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr12:1501200-1544400	Weak transcription	Right Ventricle	heart
29	chr12:1501400-1512200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr12:1501400-1516800	Weak transcription	Primary hematopoietic stem cells	blood
31	chr12:1501400-1517000	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr12:1501400-1517000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr12:1501400-1517800	Weak transcription	Stomach Smooth Muscle	stomach
34	chr12:1501400-1518000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr12:1501400-1518000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr12:1501400-1518200	Weak transcription	Fetal Intestine Large	intestine
37	chr12:1501400-1520000	Weak transcription	NHEK	skin
38	chr12:1501400-1530400	Weak transcription	Brain Substantia Nigra	brain
39	chr12:1501400-1530400	Weak transcription	Colon Smooth Muscle	Colon
40	chr12:1501600-1517400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr12:1501600-1521600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr12:1501600-1522400	Weak transcription	Brain Angular Gyrus	brain
43	chr12:1501600-1523200	Weak transcription	Fetal Intestine Small	intestine
44	chr12:1501600-1529800	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr12:1501600-1530400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr12:1501800-1530400	Weak transcription	Brain Hippocampus Middle	brain
47	chr12:1504000-1517600	Weak transcription	Left Ventricle	heart
48	chr12:1504000-1528000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr12:1504400-1517800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr12:1504400-1519600	Weak transcription	Ovary	ovary

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