Variant report

Variant	rs16928347
Chromosome Location	chr12:1416592-1416593
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:1414809..1417006-chr12:1420746..1423369,2	K562	blood:
2	chr12:1415506..1418642-chr12:1420432..1423739,3	K562	blood:
3	chr12:1414726..1416735-chr12:1417121..1420289,4	K562	blood:

Extended variants
information (count: 142 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:112)

rs_ID	r²[population]
rs1005394	0.84[CEU][hapmap];0.84[CHB][hapmap];0.88[TSI][hapmap]
rs1012719	0.88[CEU][hapmap];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10161285	0.89[CHB][hapmap]
rs10848452	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10848456	0.94[CHB][hapmap]
rs10848458	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11061677	0.96[CEU][hapmap];0.94[CHB][hapmap];0.96[CHD][hapmap];0.91[JPT][hapmap];0.94[MEX][hapmap];0.88[TSI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11061679	0.96[CEU][hapmap];0.94[CHB][hapmap];0.90[CHD][hapmap];0.90[JPT][hapmap];0.94[MEX][hapmap];0.91[TSI][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11061682	0.96[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11061691	0.96[CEU][hapmap];0.94[CHB][hapmap];0.91[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11061698	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11061699	0.89[CHB][hapmap];0.92[JPT][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11061702	0.94[CHB][hapmap];0.83[CHD][hapmap];0.84[ASN][1000 genomes]
rs11061703	0.94[CHB][hapmap];0.83[CHD][hapmap];0.84[ASN][1000 genomes]
rs11061707	0.84[CEU][hapmap];0.84[CHB][hapmap]
rs11061712	0.89[CEU][hapmap];0.84[CHB][hapmap];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11061714	0.84[CEU][hapmap];0.84[CHB][hapmap];0.84[TSI][hapmap];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11061736	0.80[CEU][hapmap]
rs11061737	0.89[CEU][hapmap];0.84[CHB][hapmap];0.84[TSI][hapmap];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11061741	0.81[CEU][hapmap]
rs11609402	0.85[ASN][1000 genomes]
rs11613252	0.81[CEU][hapmap]
rs11831980	0.87[CEU][hapmap]
rs11836372	0.81[CEU][hapmap];0.81[EUR][1000 genomes]
rs11837688	0.84[CEU][hapmap];0.84[CHB][hapmap];0.82[MEX][hapmap];0.88[TSI][hapmap]
rs12296944	0.81[CEU][hapmap]
rs12298813	0.84[CHB][hapmap];0.82[ASN][1000 genomes]
rs12301879	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12301937	0.81[CEU][hapmap]
rs12302807	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12306160	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12306260	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12307046	0.81[CEU][hapmap]
rs12308521	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12312647	0.82[CEU][hapmap]
rs12315865	0.84[EUR][1000 genomes]
rs12316687	0.81[CEU][hapmap]
rs12320911	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12321803	0.81[CEU][hapmap]
rs12423105	0.89[CEU][hapmap];0.84[CHB][hapmap];0.94[MEX][hapmap];0.91[TSI][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12424140	0.81[CEU][hapmap]
rs12426509	0.89[CHB][hapmap];0.87[CHD][hapmap]
rs1362265	0.81[CEU][hapmap]
rs1419965	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1544425	0.89[CHB][hapmap];0.93[CHD][hapmap]
rs1548805	0.81[CEU][hapmap]
rs17223448	0.84[CHB][hapmap]
rs17800876	0.89[CHB][hapmap];0.87[CHD][hapmap]
rs2051843	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2051844	0.84[CEU][hapmap];0.83[EUR][1000 genomes]
rs2189788	0.84[CHB][hapmap]
rs2286031	0.83[CHB][hapmap];0.90[CHD][hapmap]
rs2286037	0.89[CHB][hapmap];0.87[CHD][hapmap];1.00[JPT][hapmap]
rs2369701	0.82[JPT][hapmap]
rs2906109	0.91[JPT][hapmap]
rs2906112	0.82[JPT][hapmap]
rs2968874	0.91[JPT][hapmap]
rs2968882	0.82[JPT][hapmap]
rs34929071	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs41369952	0.81[CEU][hapmap]
rs56742512	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57125493	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs57707051	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs58254940	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs58639324	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs59141976	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs60222319	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61009778	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs61913073	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61913075	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs61913099	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs61913128	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6489270	0.84[CHB][hapmap]
rs6489273	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6489276	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6489277	0.96[CEU][hapmap];0.94[CHB][hapmap];0.93[CHD][hapmap];0.91[JPT][hapmap];0.94[MEX][hapmap];0.88[TSI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6489282	0.89[CEU][hapmap];0.84[CHB][hapmap];0.83[MEX][hapmap];0.91[TSI][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6489284	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7136329	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7137058	0.84[CHB][hapmap]
rs7300575	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7300981	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7303850	0.84[CHB][hapmap]
rs7306130	0.96[CEU][hapmap];0.89[CHB][hapmap];0.97[CHD][hapmap];0.92[JPT][hapmap];0.84[MEX][hapmap];0.91[TSI][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7311231	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7313311	0.84[CEU][hapmap];0.83[CHB][hapmap];0.82[MEX][hapmap];0.88[TSI][hapmap]
rs766956	0.89[CEU][hapmap];0.84[CHB][hapmap];0.94[MEX][hapmap];0.91[TSI][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs768157	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7954162	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7954213	0.84[CHB][hapmap]
rs7956588	0.88[CEU][hapmap]
rs7958662	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]
rs7961575	0.84[ASN][1000 genomes]
rs7962697	0.82[EUR][1000 genomes]
rs7963546	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7963602	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7967934	0.96[CEU][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7968223	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7968583	0.88[CEU][hapmap];0.84[CHB][hapmap];0.82[TSI][hapmap];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7968772	0.90[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7969569	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7971585	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7971670	0.89[CHB][hapmap];0.87[CHD][hapmap]
rs7972290	0.96[CEU][hapmap];0.84[CHB][hapmap];0.88[MEX][hapmap];0.95[TSI][hapmap];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7973820	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7975854	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];0.94[MEX][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7978540	0.89[CEU][hapmap];0.84[CHB][hapmap];0.82[TSI][hapmap];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7978898	0.89[CEU][hapmap];0.88[CHB][hapmap];0.81[TSI][hapmap];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7980065	0.88[CHB][hapmap];0.83[CHD][hapmap];0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs956408	0.81[CEU][hapmap]
rs9943818	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9943854	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:30 , 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	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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
30	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:83 , 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	chr12:1366600-1418000	Weak transcription	Lung	lung
4	chr12:1369400-1427600	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr12:1374200-1423200	Weak transcription	NHEK	skin
6	chr12:1375200-1419800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr12:1387400-1453400	Weak transcription	Thymus	Thymus
8	chr12:1387600-1441400	Weak transcription	HepG2	liver
9	chr12:1391200-1434000	Weak transcription	A549	lung
10	chr12:1391600-1427800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr12:1391800-1421600	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr12:1392400-1422200	Weak transcription	Ovary	ovary
13	chr12:1393200-1427400	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr12:1395200-1428000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr12:1399000-1427600	Weak transcription	Brain Angular Gyrus	brain
16	chr12:1399000-1428400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr12:1399600-1426600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr12:1400000-1427600	Weak transcription	Placenta	Placenta
19	chr12:1400400-1426800	Weak transcription	HMEC	breast
20	chr12:1400400-1427200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr12:1400400-1427200	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr12:1400600-1425200	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr12:1400800-1421400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr12:1401000-1427400	Weak transcription	HSMM	muscle
25	chr12:1401200-1418000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr12:1401200-1425400	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr12:1401200-1427200	Weak transcription	Liver	Liver
28	chr12:1401600-1427200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr12:1402600-1427800	Weak transcription	Small Intestine	intestine
30	chr12:1404800-1419400	Weak transcription	Left Ventricle	heart
31	chr12:1404800-1427400	Weak transcription	Brain Anterior Caudate	brain
32	chr12:1404800-1442600	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr12:1405000-1421400	Weak transcription	Fetal Thymus	thymus
34	chr12:1405000-1422200	Weak transcription	Primary B cells from peripheral blood	blood
35	chr12:1407000-1427600	Weak transcription	Fetal Kidney	kidney
36	chr12:1407200-1418000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr12:1407800-1424200	Weak transcription	Fetal Stomach	stomach
38	chr12:1409600-1423400	Weak transcription	Fetal Brain Female	brain
39	chr12:1409600-1424000	Weak transcription	Fetal Intestine Large	intestine
40	chr12:1409600-1424200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
41	chr12:1410000-1420000	Weak transcription	Fetal Lung	lung
42	chr12:1410200-1426800	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr12:1410600-1426800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr12:1410800-1427200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr12:1412000-1428000	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr12:1412800-1420000	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr12:1413400-1416600	Enhancers	Fetal Heart	heart
48	chr12:1413600-1416600	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr12:1413800-1424200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr12:1413800-1427400	Weak transcription	Brain Substantia Nigra	brain

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