Variant report

Variant	rs7980065
Chromosome Location	chr12:1347086-1347087
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	chr12:1345086..1347706-chr12:1348677..1351190,2	K562	blood:

Extended variants
information (count: 129 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs1005394	0.81[CHB][hapmap]
rs10161285	1.00[CHB][hapmap];0.85[JPT][hapmap];0.93[ASN][1000 genomes]
rs1017019	0.95[ASN][1000 genomes]
rs10848442	0.83[CEU][hapmap]
rs10848452	0.87[ASN][1000 genomes]
rs10848456	0.94[CHB][hapmap];0.93[JPT][hapmap]
rs11061677	0.94[CHB][hapmap];0.90[CHD][hapmap];0.87[ASN][1000 genomes]
rs11061679	0.94[CHB][hapmap];0.80[CHD][hapmap];0.87[ASN][1000 genomes]
rs11061682	0.94[CHB][hapmap];0.87[ASN][1000 genomes]
rs11061691	0.94[CHB][hapmap];0.82[ASN][1000 genomes]
rs11061698	0.80[ASN][1000 genomes]
rs11061699	0.83[CHB][hapmap]
rs11061702	0.94[CHB][hapmap];1.00[JPT][hapmap]
rs11061703	0.94[CHB][hapmap];0.85[JPT][hapmap]
rs11061707	0.81[CHB][hapmap]
rs11061712	0.81[CHB][hapmap]
rs11061714	0.81[CHB][hapmap];0.81[GIH][hapmap]
rs11061737	0.81[CHB][hapmap];0.81[GIH][hapmap];0.81[MEX][hapmap]
rs11835033	0.95[ASN][1000 genomes]
rs11837033	0.84[ASN][1000 genomes]
rs11837688	0.81[CHB][hapmap]
rs11837972	0.87[ASN][1000 genomes]
rs12298813	0.81[CHB][hapmap];0.88[GIH][hapmap];0.85[MEX][hapmap]
rs12302807	0.87[ASN][1000 genomes]
rs12306160	0.80[ASN][1000 genomes]
rs12315865	0.80[ASN][1000 genomes]
rs12423105	0.81[CHB][hapmap]
rs12426509	1.00[CHB][hapmap];0.90[CHD][hapmap];0.85[JPT][hapmap];0.95[ASN][1000 genomes]
rs1544425	1.00[CHB][hapmap];0.83[CHD][hapmap];0.85[JPT][hapmap];0.95[ASN][1000 genomes]
rs16928347	0.88[CHB][hapmap];0.83[CHD][hapmap];0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs17223448	0.94[CHB][hapmap];0.83[CHD][hapmap];0.85[JPT][hapmap]
rs17800876	1.00[CHB][hapmap];0.90[CHD][hapmap];0.85[JPT][hapmap];0.91[ASN][1000 genomes]
rs2189788	0.94[CHB][hapmap];0.83[CHD][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs2286031	0.94[CHB][hapmap];0.80[CHD][hapmap];0.81[GIH][hapmap];0.85[MEX][hapmap];0.80[TSI][hapmap];0.83[ASN][1000 genomes]
rs2286037	1.00[CHB][hapmap];0.90[CHD][hapmap];0.90[ASN][1000 genomes]
rs2369701	0.82[CHB][hapmap]
rs2906109	0.88[CHB][hapmap]
rs2968874	0.88[CHB][hapmap]
rs2968882	0.82[CHB][hapmap]
rs3924361	0.81[CEU][hapmap];0.80[GIH][hapmap];0.92[MKK][hapmap]
rs4511332	0.81[CHB][hapmap]
rs4766249	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56742512	0.87[ASN][1000 genomes]
rs57027936	0.90[ASN][1000 genomes]
rs57389981	0.86[ASN][1000 genomes]
rs58159804	0.95[ASN][1000 genomes]
rs58545225	0.90[ASN][1000 genomes]
rs60257878	0.92[ASN][1000 genomes]
rs61623983	0.84[ASN][1000 genomes]
rs61911966	0.92[ASN][1000 genomes]
rs61911969	0.92[ASN][1000 genomes]
rs61911972	0.92[ASN][1000 genomes]
rs61911976	0.88[ASN][1000 genomes]
rs61911977	0.88[ASN][1000 genomes]
rs61911978	0.88[ASN][1000 genomes]
rs61911983	0.90[ASN][1000 genomes]
rs61911984	0.90[ASN][1000 genomes]
rs61912026	0.90[ASN][1000 genomes]
rs61913073	0.80[ASN][1000 genomes]
rs61914332	0.87[ASN][1000 genomes]
rs6489270	0.94[CHB][hapmap];0.83[CHD][hapmap];0.85[JPT][hapmap];0.87[ASN][1000 genomes]
rs6489273	0.88[ASN][1000 genomes]
rs6489276	0.89[ASN][1000 genomes]
rs6489277	0.94[CHB][hapmap];0.90[CHD][hapmap];0.87[ASN][1000 genomes]
rs6489282	0.81[CHB][hapmap]
rs7133150	0.82[ASN][1000 genomes]
rs7137058	0.94[CHB][hapmap];0.83[CHD][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs7137563	0.84[ASN][1000 genomes]
rs7299878	0.84[ASN][1000 genomes]
rs7300575	0.88[CHB][hapmap];0.83[CHD][hapmap];0.85[JPT][hapmap];0.80[ASN][1000 genomes]
rs7300981	0.80[ASN][1000 genomes]
rs7303756	0.82[ASN][1000 genomes]
rs7303850	0.94[CHB][hapmap];0.83[CHD][hapmap];0.85[JPT][hapmap];0.87[ASN][1000 genomes]
rs7306130	0.88[CHB][hapmap];0.87[CHD][hapmap];0.89[ASN][1000 genomes]
rs7311531	0.84[ASN][1000 genomes]
rs7313311	0.81[CHB][hapmap]
rs7315544	0.92[ASN][1000 genomes]
rs766956	0.81[CHB][hapmap]
rs7954213	0.94[CHB][hapmap];0.85[JPT][hapmap];0.84[ASN][1000 genomes]
rs7958662	0.94[CHB][hapmap];0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs7963602	0.81[ASN][1000 genomes]
rs7968223	0.82[ASN][1000 genomes]
rs7968583	0.81[CHB][hapmap];0.81[GIH][hapmap];0.80[MEX][hapmap]
rs7971585	0.81[ASN][1000 genomes]
rs7971670	1.00[CHB][hapmap];0.90[CHD][hapmap];0.85[JPT][hapmap];0.92[ASN][1000 genomes]
rs7972290	0.81[CHB][hapmap]
rs7975854	0.88[CHB][hapmap];0.83[CHD][hapmap];0.85[JPT][hapmap];0.80[ASN][1000 genomes]
rs7976337	0.95[ASN][1000 genomes]
rs7978540	0.81[CHB][hapmap];0.81[GIH][hapmap];0.81[MEX][hapmap]
rs7978898	0.81[CHB][hapmap];0.81[GIH][hapmap];0.80[MEX][hapmap]
rs7980582	0.95[ASN][1000 genomes]
rs979335	0.84[ASN][1000 genomes]
rs9943818	0.88[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:36 , 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	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	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
25	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
26	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
27	nsv524525	chr12:1272363-1366511	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
28	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
29	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
30	esv1839295	chr12:1305357-1372114	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
31	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
32	nsv519502	chr12:1314430-1366511	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
33	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
34	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
35	esv1836738	chr12:1344141-1374396	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
36	esv1838583	chr12:1344141-1374396	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1316800-1366200	Weak transcription	Primary B cells from cord blood	blood
2	chr12:1327200-1391200	Weak transcription	Aorta	Aorta
3	chr12:1327600-1352400	Weak transcription	HSMM	muscle
4	chr12:1327600-1354200	Weak transcription	Osteobl	bone
5	chr12:1327800-1348400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr12:1328000-1359200	Weak transcription	HUVEC	blood vessel
7	chr12:1329200-1366200	Weak transcription	Lung	lung
8	chr12:1330200-1348200	Weak transcription	Fetal Muscle Trunk	muscle
9	chr12:1330200-1348200	Weak transcription	Fetal Stomach	stomach
10	chr12:1330200-1353800	Weak transcription	Pancreas	Pancrea
11	chr12:1330200-1358800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr12:1330200-1390600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr12:1330200-1391400	Weak transcription	Fetal Muscle Leg	muscle
14	chr12:1330400-1372200	Weak transcription	Stomach Smooth Muscle	stomach
15	chr12:1330400-1373200	Weak transcription	Hela-S3	cervix
16	chr12:1334200-1425000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr12:1335800-1352600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr12:1336000-1360400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr12:1337800-1347800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr12:1339800-1358600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr12:1341400-1348200	Weak transcription	Ovary	ovary
22	chr12:1341400-1373000	Weak transcription	Fetal Intestine Small	intestine
23	chr12:1341800-1347800	Weak transcription	Dnd41	blood
24	chr12:1341800-1420000	Weak transcription	Esophagus	oesophagus
25	chr12:1342000-1359200	Weak transcription	Fetal Lung	lung
26	chr12:1343000-1359000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr12:1343600-1350600	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr12:1343600-1358800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr12:1343600-1359000	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr12:1343600-1372000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr12:1343600-1372000	Weak transcription	Fetal Heart	heart
32	chr12:1343600-1378000	Weak transcription	Gastric	stomach
33	chr12:1343600-1381400	Weak transcription	Right Ventricle	heart
34	chr12:1343600-1390600	Weak transcription	NHLF	lung
35	chr12:1343600-1398800	Weak transcription	Brain Cingulate Gyrus	brain
36	chr12:1343800-1377800	Weak transcription	A549	lung
37	chr12:1343800-1390800	Weak transcription	HSMMtube	muscle
38	chr12:1344000-1348200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr12:1344000-1359800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr12:1344200-1358800	Weak transcription	NHEK	skin
41	chr12:1344200-1359000	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr12:1344400-1355400	Weak transcription	Thymus	Thymus
43	chr12:1344600-1358800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr12:1344800-1349000	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr12:1344800-1375000	Weak transcription	Fetal Thymus	thymus
46	chr12:1345000-1382800	Weak transcription	Spleen	Spleen
47	chr12:1345400-1359200	Weak transcription	Brain Angular Gyrus	brain
48	chr12:1345800-1347200	Strong transcription	Primary T cells from cord blood	blood
49	chr12:1345800-1347200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr12:1345800-1347200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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