Variant report

Variant	rs12812965
Chromosome Location	chr12:1163518-1163519
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	chr12:1161679..1164344-chr12:1168247..1169852,2	MCF-7	breast:
2	chr12:1157626..1159829-chr12:1163516..1166184,2	K562	blood:

Extended variants
information (count: 108 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs10400515	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10505719	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10505720	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11831674	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11833070	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11834340	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11835502	0.91[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11836039	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11837382	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11837384	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12812586	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12814466	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12817140	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12817182	0.86[CHB][hapmap];0.82[JPT][hapmap];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12817372	0.96[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12817987	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12822249	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12824693	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12827694	0.96[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.91[ASN][1000 genomes]
rs1344443	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1345238	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs16932084	0.88[CHB][hapmap]
rs17694207	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17694270	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17755839	1.00[CHB][hapmap];0.85[JPT][hapmap];0.91[ASN][1000 genomes]
rs17755993	0.94[EUR][1000 genomes]
rs17756029	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2369668	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34076252	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34186162	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34213826	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34527943	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34548540	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34860455	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34999895	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35092149	0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35562585	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35580664	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35586095	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35619011	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35681937	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35738441	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35802047	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35821403	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs36011250	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36054627	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4459369	0.87[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap]
rs59462516	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61917252	0.82[ASN][1000 genomes]
rs61917256	0.85[ASN][1000 genomes]
rs61917258	0.85[ASN][1000 genomes]
rs61917259	0.87[ASN][1000 genomes]
rs61918689	0.87[ASN][1000 genomes]
rs61918690	0.84[ASN][1000 genomes]
rs61918691	0.87[ASN][1000 genomes]
rs61918693	0.91[ASN][1000 genomes]
rs61918695	0.91[ASN][1000 genomes]
rs61918696	0.91[ASN][1000 genomes]
rs61918698	0.93[ASN][1000 genomes]
rs61918699	0.91[ASN][1000 genomes]
rs61918702	0.87[ASN][1000 genomes]
rs61918703	0.91[ASN][1000 genomes]
rs61918736	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61918737	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61918740	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61918741	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61918742	0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs61918747	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61918748	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7132220	0.96[CEU][hapmap];0.88[CHB][hapmap];0.86[JPT][hapmap];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7298537	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7298929	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73035153	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7314200	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs73606385	0.83[ASN][1000 genomes]
rs73606388	0.91[ASN][1000 genomes]
rs7954090	0.89[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.90[ASN][1000 genomes]
rs7977736	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7980813	0.94[EUR][1000 genomes];0.90[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	nsv1049944	chr12:282465-1232077	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer 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	80 gene(s)	inside rSNPs	diseases
2	nsv541306	chr12:282465-1232077	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
3	nsv556892	chr12:673515-1210884	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	nsv492321	chr12:1011692-1388512	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS 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 miRNA target site	33 gene(s)	inside rSNPs	diseases
15	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
16	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
17	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
18	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
19	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
20	nsv868854	chr12:1045935-1354083	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
21	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
22	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
23	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
24	nsv1041799	chr12:1091294-1304839	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
25	nsv541343	chr12:1091294-1304839	Flanking Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
26	nsv468963	chr12:1106783-1220688	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
27	nsv556943	chr12:1106783-1220688	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
28	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
29	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

No data

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1137600-1164400	Weak transcription	Gastric	stomach
2	chr12:1137600-1172200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr12:1137800-1167400	Weak transcription	Lung	lung
4	chr12:1137800-1172200	Weak transcription	Aorta	Aorta
5	chr12:1138000-1166600	Weak transcription	Fetal Muscle Trunk	muscle
6	chr12:1138000-1172200	Weak transcription	Placenta	Placenta
7	chr12:1138200-1164200	Weak transcription	Primary B cells from peripheral blood	blood
8	chr12:1138600-1167000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr12:1139800-1169400	Weak transcription	Fetal Thymus	thymus
10	chr12:1140200-1167400	Weak transcription	Primary B cells from cord blood	blood
11	chr12:1149400-1166400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr12:1151400-1168000	Weak transcription	Fetal Stomach	stomach
13	chr12:1153400-1200400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr12:1154400-1167600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr12:1154600-1163800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr12:1154800-1163600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr12:1156800-1164000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr12:1157600-1163600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr12:1157600-1165600	Weak transcription	Right Atrium	heart
20	chr12:1157600-1171600	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr12:1157600-1171800	Weak transcription	Thymus	Thymus
22	chr12:1157600-1171800	Weak transcription	Osteobl	bone
23	chr12:1157600-1172000	Weak transcription	Left Ventricle	heart
24	chr12:1157600-1172000	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr12:1157600-1172200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr12:1157800-1163600	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr12:1157800-1163600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr12:1157800-1167400	Weak transcription	NHEK	skin
29	chr12:1157800-1167800	Weak transcription	Fetal Muscle Leg	muscle
30	chr12:1157800-1167800	Weak transcription	Sigmoid Colon	Sigmoid Colon
31	chr12:1158000-1163600	Weak transcription	Pancreas	Pancrea
32	chr12:1158000-1171400	Weak transcription	Primary T cells from cord blood	blood
33	chr12:1158400-1163600	Weak transcription	Adipose Nuclei	Adipose
34	chr12:1159600-1165600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr12:1159600-1165800	Weak transcription	HMEC	breast
36	chr12:1159600-1167200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr12:1159600-1167800	Weak transcription	Primary hematopoietic stem cells	blood
38	chr12:1159800-1171600	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr12:1160000-1167400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr12:1160800-1166200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr12:1161400-1171600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr12:1161600-1163600	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr12:1161600-1164200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr12:1161800-1165400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr12:1162200-1164200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr12:1162200-1164200	Enhancers	Brain Anterior Caudate	brain
47	chr12:1162200-1164600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr12:1162200-1167000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr12:1162400-1163600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr12:1162400-1163800	Enhancers	Ovary	ovary

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links