Variant report

Variant	rs7077970
Chromosome Location	chr10:55400840-55400841
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 120 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10762997	0.81[ASN][1000 genomes]
rs10762999	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10825074	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10825078	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10825079	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10825081	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10825082	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10825083	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10825084	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10825085	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10825086	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10825087	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10825088	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10825089	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11003708	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11003709	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11003724	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11003726	0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11003727	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11003731	0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11003740	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11003743	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11003745	0.85[EUR][1000 genomes]
rs11003746	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11003747	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11003748	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11003749	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11003750	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11003751	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11003752	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11003753	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11003754	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11003755	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11003756	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11003762	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11003786	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11814564	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12412315	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12412620	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12416362	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12776465	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12778875	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12781314	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1343016	0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1489824	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1489828	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1489836	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1602162	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1686678	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1686679	0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16937617	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1825794	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2153948	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2153949	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2153950	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2185842	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2384268	0.84[EUR][1000 genomes]
rs2384269	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2384300	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2384301	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2451318	0.88[ASN][1000 genomes]
rs4607982	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4935081	0.85[EUR][1000 genomes]
rs4935082	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4935454	0.95[ASN][1000 genomes]
rs57372970	0.87[EUR][1000 genomes]
rs59556125	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61859909	0.87[EUR][1000 genomes]
rs7067829	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7096810	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs721276	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7906396	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs825805	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9416279	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9416280	0.90[EUR][1000 genomes]
rs9416283	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9416284	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9416287	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9416289	0.94[ASN][1000 genomes]
rs9988661	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:40 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752952	chr10:54900994-55497594	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1044282	chr10:55186501-55516392	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv540631	chr10:55186501-55516392	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1043501	chr10:55186701-55516253	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv540632	chr10:55186701-55516253	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1050323	chr10:55190079-55546575	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	esv2757386	chr10:55357136-55531037	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	esv2759753	chr10:55357136-55586930	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	esv2758220	chr10:55360612-55586930	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv1047468	chr10:55361202-55459392	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv515498	chr10:55371601-55454152	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
12	esv1847684	chr10:55371601-55638740	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv8666	chr10:55371860-55459830	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv1044236	chr10:55372005-55426888	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv1040454	chr10:55372005-55457884	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv467208	chr10:55378668-55423964	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv550932	chr10:55378668-55423964	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
18	nsv470941	chr10:55378668-55454151	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	esv3693056	chr10:55378668-55454152	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
20	nsv438174	chr10:55378668-55454152	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
21	esv1842975	chr10:55378668-55736655	ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
22	nsv1054744	chr10:55379719-55456587	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
23	nsv1051388	chr10:55379719-55457393	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
24	nsv1053647	chr10:55379719-55457884	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
25	nsv1043179	chr10:55379719-55463942	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
26	esv2760118	chr10:55379731-55457896	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
27	nsv1035366	chr10:55380381-55457306	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
28	nsv1046336	chr10:55380381-55457884	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
29	esv34540	chr10:55383168-55457394	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
30	esv34353	chr10:55383168-55479314	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
31	nsv895410	chr10:55385962-55577022	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
32	nsv895411	chr10:55390656-55417666	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
33	esv2755263	chr10:55394094-55546994	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
34	nsv550933	chr10:55395318-55405696	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
35	nsv895412	chr10:55395380-55418087	Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
36	nsv895413	chr10:55395380-55446058	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
37	nsv895414	chr10:55395380-55449214	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
38	nsv895415	chr10:55395380-55473976	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
39	nsv895416	chr10:55395380-55539954	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
40	nsv895417	chr10:55396233-55413116	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:55398400-55403200	Weak transcription	Fetal Lung	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links