Variant report

Variant	rs4432082
Chromosome Location	chr12:38250212-38250213
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 235 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:102)

rs_ID	r²[population]
rs11177197	0.89[AFR][1000 genomes]
rs11177200	0.85[AFR][1000 genomes]
rs11178953	0.81[AMR][1000 genomes]
rs11179135	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs11179436	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs11179536	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs11179579	0.88[AMR][1000 genomes]
rs11179830	0.90[AMR][1000 genomes]
rs11180482	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11180504	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11180549	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11180579	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11180821	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11180825	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11181245	0.85[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs11495369	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11495374	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs11495375	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs11495648	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs11495668	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs11495699	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs11514040	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs11514056	0.81[AMR][1000 genomes]
rs11514282	0.85[AFR][1000 genomes]
rs11514289	0.85[AFR][1000 genomes]
rs11514339	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11514342	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11514348	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11514349	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11514352	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11519905	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs11519907	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs11519926	0.82[AMR][1000 genomes]
rs11520165	0.89[AFR][1000 genomes]
rs11520191	0.81[AMR][1000 genomes]
rs11520195	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs11520199	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs11520201	0.84[AMR][1000 genomes]
rs11520218	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs11520237	0.85[AMR][1000 genomes]
rs11522893	0.89[AFR][1000 genomes]
rs11522896	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11522898	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs11522899	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs11525001	0.89[AMR][1000 genomes]
rs11612125	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs11613378	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs11613836	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs12146734	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12366709	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs12368410	0.80[AMR][1000 genomes]
rs12368485	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12368889	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs12370589	0.85[AFR][1000 genomes]
rs12370982	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs12371948	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12372025	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs12372514	0.90[AFR][1000 genomes]
rs12372810	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs12810027	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs12824232	0.85[AFR][1000 genomes]
rs2320449	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs2320521	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2320522	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2320523	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2320526	0.90[AMR][1000 genomes]
rs2320745	0.90[AMR][1000 genomes]
rs2387317	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2874289	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2874290	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2874292	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs2874343	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs34438288	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs34460744	0.95[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs34917043	0.95[AFR][1000 genomes]
rs3898237	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes]
rs3900361	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs3910796	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4002580	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes]
rs4516042	0.80[AMR][1000 genomes]
rs4556621	0.95[AFR][1000 genomes]
rs55962152	0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs66545149	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs67792345	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs67889662	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7294298	0.80[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs7294300	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7294305	0.84[AMR][1000 genomes]
rs7305409	0.82[AMR][1000 genomes]
rs7308714	0.84[AMR][1000 genomes]
rs7311462	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs7312212	0.80[AMR][1000 genomes]
rs8189445	0.81[AMR][1000 genomes]
rs8189464	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs8189467	0.90[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs8189486	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8189516	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs8189549	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8189597	0.85[AMR][1000 genomes]
rs8189609	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs8189618	0.81[AMR][1000 genomes]
rs8189620	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:133 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv976600	chr12:37856695-38447701	ZNF genes & repeats Bivalent/Poised TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1048715	chr12:37857751-38283657	Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1043459	chr12:37857751-38662460	ZNF genes & repeats Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv1050718	chr12:37857751-38757302	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	nsv898972	chr12:37857899-38719455	ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
6	nsv558348	chr12:37860597-38424982	ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	esv2754312	chr12:37890833-38424933	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv898973	chr12:37913469-38733094	Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
9	nsv898974	chr12:37913469-38881918	ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
10	nsv1035849	chr12:37929227-38640613	ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	nsv470284	chr12:37933454-38381046	Active TSS Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
12	nsv527488	chr12:37933454-38432009	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	nsv1041772	chr12:37961768-38353859	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
14	nsv898975	chr12:37964922-38499180	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
15	nsv898976	chr12:37964922-38640613	Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
16	nsv1052311	chr12:37966307-38393648	ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
17	nsv1049306	chr12:37966307-38437819	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
18	nsv898977	chr12:37969625-38472919	ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
19	nsv898978	chr12:37969625-38624795	Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
20	nsv1037148	chr12:37971619-38346916	ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
21	nsv508671	chr12:37973300-38273345	ZNF genes & repeats Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
22	nsv898979	chr12:37986081-38446861	Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
23	nsv898980	chr12:37986081-38446861	Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
24	nsv1051611	chr12:37987714-38292067	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
25	nsv1043150	chr12:37987714-38346916	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
26	nsv1047523	chr12:37987714-38393648	ZNF genes & repeats Weak transcription Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
27	nsv1041403	chr12:37987714-38439587	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
28	nsv1050465	chr12:37987714-38479611	Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
29	esv13222	chr12:37990409-38450414	ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
30	nsv820975	chr12:37990409-38450414	ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
31	nsv558368	chr12:37992511-38269222	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
32	nsv558369	chr12:37992511-38420405	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
33	nsv558370	chr12:37992511-38444056	ZNF genes & repeats Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
34	nsv558378	chr12:37992615-38385834	Bivalent Enhancer ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
35	nsv558422	chr12:37993759-38420380	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
36	nsv558426	chr12:37993928-38420380	Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
37	nsv558427	chr12:37993928-38420405	ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
38	nsv558430	chr12:37995364-38420405	ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
39	nsv558436	chr12:37998071-38420405	Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
40	nsv558484	chr12:38008984-38252147	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
41	nsv558485	chr12:38008984-38258137	Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
42	nsv558491	chr12:38009843-38253043	Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
43	nsv558492	chr12:38009843-38253789	Weak transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
44	nsv558493	chr12:38009843-38258137	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
45	nsv558494	chr12:38009843-38263084	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
46	nsv558495	chr12:38009843-38278512	Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
47	nsv558503	chr12:38010350-38263084	ZNF genes & repeats Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
48	nsv558523	chr12:38011409-38250905	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
49	nsv558524	chr12:38011409-38258137	Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
50	nsv558525	chr12:38011409-38263084	Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:38248800-38251000	Weak transcription	Aorta	Aorta
2	chr12:38248800-38251200	Weak transcription	Fetal Heart	heart
3	chr12:38248800-38253000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr12:38248800-38253000	Weak transcription	Fetal Kidney	kidney
5	chr12:38248800-38253200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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