Variant report

Variant	rs7300575
Chromosome Location	chr12:1429190-1429191
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:1428172..1430846-chr12:1431367..1432976,2	K562	blood:

Extended variants
information (count: 143 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:114)

rs_ID	r²[population]
rs1005394	0.88[CEU][hapmap];0.84[CHB][hapmap];0.83[ASN][1000 genomes]
rs1012719	0.92[CEU][hapmap];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10161285	0.89[CHB][hapmap]
rs10848452	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10848456	0.94[CHB][hapmap]
rs10848458	0.99[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];0.97[GIH][hapmap];0.92[JPT][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11061679	0.96[CEU][hapmap];0.94[CHB][hapmap];0.90[CHD][hapmap];0.97[GIH][hapmap];0.92[JPT][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11061682	0.96[CEU][hapmap];0.94[CHB][hapmap];0.92[JPT][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11061691	0.96[CEU][hapmap];0.94[CHB][hapmap];0.92[JPT][hapmap];0.93[YRI][hapmap];0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11061698	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11061699	0.89[CHB][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11061702	0.94[CHB][hapmap];0.86[CHD][hapmap];0.86[ASN][1000 genomes]
rs11061703	0.94[CHB][hapmap];0.83[CHD][hapmap];0.86[ASN][1000 genomes]
rs11061705	0.83[ASN][1000 genomes]
rs11061707	0.88[CEU][hapmap];0.84[CHB][hapmap];0.83[ASN][1000 genomes]
rs11061712	0.88[CEU][hapmap];0.84[CHB][hapmap];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11061714	0.84[CEU][hapmap];0.84[CHB][hapmap];0.85[GIH][hapmap];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11061736	0.80[CEU][hapmap]
rs11061737	0.88[CEU][hapmap];0.84[CHB][hapmap];0.85[GIH][hapmap];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11061741	0.81[CEU][hapmap]
rs11609402	0.85[ASN][1000 genomes]
rs11613252	0.81[CEU][hapmap]
rs11831980	0.86[CEU][hapmap]
rs11836372	0.80[CEU][hapmap];0.81[EUR][1000 genomes]
rs11837688	0.88[CEU][hapmap];0.84[CHB][hapmap];0.83[ASN][1000 genomes]
rs12296944	0.81[CEU][hapmap]
rs12298813	0.81[CEU][hapmap];0.84[CHB][hapmap];0.81[GIH][hapmap];0.84[ASN][1000 genomes]
rs12301879	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12301937	0.81[CEU][hapmap]
rs12302807	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12306160	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12306260	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12307046	0.81[CEU][hapmap]
rs12308521	0.81[EUR][1000 genomes];0.84[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];0.88[ASN][1000 genomes]
rs12321803	0.81[CEU][hapmap]
rs12423105	0.92[CEU][hapmap];0.84[CHB][hapmap];0.95[GIH][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12424140	0.80[CEU][hapmap]
rs12426509	0.89[CHB][hapmap];0.83[CHD][hapmap]
rs1362265	0.81[CEU][hapmap]
rs1419965	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1544425	0.89[CHB][hapmap];0.90[CHD][hapmap]
rs1548805	0.81[CEU][hapmap]
rs16928347	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]
rs17223448	0.84[CHB][hapmap]
rs17800876	0.89[CHB][hapmap];0.83[CHD][hapmap]
rs2051843	0.85[EUR][1000 genomes];0.84[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];0.83[CHD][hapmap];0.84[JPT][hapmap]
rs34929071	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35579512	0.83[ASN][1000 genomes]
rs41369952	0.81[CEU][hapmap]
rs56742512	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs57125493	0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs57707051	0.85[EUR][1000 genomes];0.84[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];0.88[ASN][1000 genomes]
rs59141976	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs60222319	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61009778	0.88[EUR][1000 genomes]
rs61913073	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61913075	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61913097	0.83[ASN][1000 genomes]
rs61913099	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs61913128	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6489270	0.84[CHB][hapmap]
rs6489273	0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6489276	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6489277	0.96[CEU][hapmap];0.94[CHB][hapmap];0.93[CHD][hapmap];0.97[GIH][hapmap];0.92[JPT][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6489282	0.92[CEU][hapmap];0.84[CHB][hapmap];0.95[GIH][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6489284	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7136329	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7137058	0.84[CHB][hapmap]
rs7300981	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7303850	0.84[CHB][hapmap]
rs73038635	0.83[ASN][1000 genomes]
rs73038647	0.83[ASN][1000 genomes]
rs7306130	0.96[CEU][hapmap];0.89[CHB][hapmap];0.96[CHD][hapmap];0.97[GIH][hapmap];0.92[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7311231	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7313311	0.88[CEU][hapmap];0.83[CHB][hapmap];0.83[ASN][1000 genomes]
rs766956	0.92[CEU][hapmap];0.84[CHB][hapmap];0.95[GIH][hapmap];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs768157	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7954162	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7954213	0.84[CHB][hapmap]
rs7956588	0.92[CEU][hapmap];0.83[ASN][1000 genomes]
rs7956798	0.83[ASN][1000 genomes]
rs7958662	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]
rs7961575	0.86[ASN][1000 genomes]
rs7962697	0.82[EUR][1000 genomes]
rs7963546	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7963602	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7967934	0.96[CEU][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7968223	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7968583	0.88[CEU][hapmap];0.84[CHB][hapmap];0.85[GIH][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7968772	0.90[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7969569	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7971585	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7971670	0.89[CHB][hapmap];0.83[CHD][hapmap]
rs7972088	0.83[ASN][1000 genomes]
rs7972290	0.96[CEU][hapmap];0.84[CHB][hapmap];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7973820	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7975854	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][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]
rs7978540	0.88[CEU][hapmap];0.84[CHB][hapmap];0.85[GIH][hapmap];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7978898	0.88[CEU][hapmap];0.88[CHB][hapmap];0.85[GIH][hapmap];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7980065	0.88[CHB][hapmap];0.83[CHD][hapmap];0.85[JPT][hapmap];0.80[ASN][1000 genomes]
rs956408	0.81[CEU][hapmap]
rs9943818	0.96[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9943854	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:29 , 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	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	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
28	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
29	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

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1387400-1453400	Weak transcription	Thymus	Thymus
2	chr12:1387600-1441400	Weak transcription	HepG2	liver
3	chr12:1391200-1434000	Weak transcription	A549	lung
4	chr12:1404800-1442600	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr12:1413800-1447600	Weak transcription	Gastric	stomach
6	chr12:1416200-1434400	Weak transcription	Fetal Muscle Trunk	muscle
7	chr12:1416400-1434000	Weak transcription	Primary hematopoietic stem cells	blood
8	chr12:1420200-1440600	Weak transcription	Primary T cells from cord blood	blood
9	chr12:1423000-1435400	Weak transcription	Fetal Thymus	thymus
10	chr12:1424400-1432200	Weak transcription	Primary B cells from cord blood	blood
11	chr12:1424400-1433400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr12:1424800-1442200	Weak transcription	Fetal Stomach	stomach
13	chr12:1427800-1429200	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr12:1428000-1442200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr12:1428000-1447600	Weak transcription	Ovary	ovary
16	chr12:1428200-1429600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr12:1428200-1433200	Weak transcription	K562	blood
18	chr12:1428200-1434000	Weak transcription	Small Intestine	intestine
19	chr12:1428200-1441600	Weak transcription	Pancreas	Pancrea
20	chr12:1428200-1442800	Weak transcription	Fetal Muscle Leg	muscle
21	chr12:1428200-1443200	Weak transcription	Fetal Brain Female	brain
22	chr12:1428200-1447600	Weak transcription	Left Ventricle	heart
23	chr12:1428200-1448800	Weak transcription	Psoas Muscle	Psoas
24	chr12:1428200-1449000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr12:1428200-1449000	Weak transcription	Aorta	Aorta
26	chr12:1428200-1455000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr12:1428200-1500400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
28	chr12:1428400-1429200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr12:1428400-1429200	Enhancers	Rectal Smooth Muscle	rectum
30	chr12:1428400-1432800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr12:1428400-1433000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr12:1428400-1433000	Weak transcription	Fetal Brain Male	brain
33	chr12:1428400-1436400	Weak transcription	Fetal Heart	heart
34	chr12:1428400-1438800	Weak transcription	Fetal Intestine Small	intestine
35	chr12:1428400-1438800	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr12:1428400-1440600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr12:1428400-1440800	Weak transcription	Brain Angular Gyrus	brain
38	chr12:1428600-1430600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr12:1428600-1431000	Weak transcription	Primary monocytes fromperipheralblood	blood
40	chr12:1428600-1434000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr12:1428600-1434200	Weak transcription	Brain Anterior Caudate	brain
42	chr12:1428600-1440400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr12:1428600-1440400	Weak transcription	NHEK	skin
44	chr12:1428600-1441200	Weak transcription	Brain Germinal Matrix	brain
45	chr12:1428800-1429400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr12:1428800-1431200	Weak transcription	HSMM	muscle
47	chr12:1428800-1431600	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr12:1428800-1433800	Weak transcription	Colon Smooth Muscle	Colon
49	chr12:1428800-1434200	Weak transcription	Adipose Nuclei	Adipose
50	chr12:1429000-1429200	Enhancers	Breast Myoepithelial Primary Cells	Breast

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