Variant report

Variant	rs62140728
Chromosome Location	chr2:51520023-51520024
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 114 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs10490140	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10490142	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10490144	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10490146	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10490147	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10490148	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10490149	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10490151	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11125342	1.00[ASN][1000 genomes]
rs11685985	1.00[ASN][1000 genomes]
rs12990508	1.00[ASN][1000 genomes]
rs17041430	1.00[ASN][1000 genomes]
rs17588430	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17588666	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17588882	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17588966	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2353318	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34437868	1.00[ASN][1000 genomes]
rs35941079	1.00[ASN][1000 genomes]
rs4998140	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4998141	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4998143	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4998144	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs55653342	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62140692	1.00[ASN][1000 genomes]
rs62140695	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140697	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140698	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs62140699	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140700	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140701	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140702	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140721	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140722	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140723	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140724	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140725	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs62140726	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140727	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140729	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140730	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140731	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140732	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62140737	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62140744	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62140745	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62140746	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62140747	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62140748	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62142867	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62142868	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62142869	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62142871	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62142872	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62142873	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62142874	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62142875	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62142876	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62142877	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62142879	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62142880	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62142883	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62142884	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62142885	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62142886	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62142887	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6709031	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72832108	1.00[ASN][1000 genomes]
rs72832136	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72832138	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72832139	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72832141	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs72832143	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72832145	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72832146	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72832147	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72832163	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72832165	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72832170	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72832172	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72832179	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7563048	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7576159	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7576370	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7579154	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7579241	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7602731	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7602908	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7602955	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932208	chr2:50847100-51556715	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv915824	chr2:50978466-51528474	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv581853	chr2:51013647-51554047	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1014907	chr2:51074517-51532889	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1007188	chr2:51135645-51821787	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv535704	chr2:51135645-51821787	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv1005168	chr2:51142848-51702008	Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats 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	8 gene(s)	inside rSNPs	diseases
8	nsv535705	chr2:51142848-51702008	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv948449	chr2:51152019-51735494	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv948354	chr2:51188566-51521625	Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv1001552	chr2:51225970-52139741	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
12	nsv535708	chr2:51225970-52139741	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
13	nsv1004239	chr2:51226169-51606258	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv535709	chr2:51226169-51606258	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
15	nsv491634	chr2:51226170-51556715	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
16	nsv874057	chr2:51294096-51606559	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
17	nsv530834	chr2:51314371-51556715	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
18	nsv1011583	chr2:51382812-51702008	Enhancers Bivalent/Poised TSS 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
19	nsv535711	chr2:51382812-51702008	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
20	nsv874063	chr2:51479170-51520327	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
21	nsv874064	chr2:51492973-51594480	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
22	nsv821624	chr2:51513925-51844864	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
23	esv2760590	chr2:51517041-51525025	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
24	nsv518215	chr2:51517775-51520327	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	inside rSNPs	diseases
25	esv1841147	chr2:51519281-51569503	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:51517000-51520200	Weak transcription	Liver	Liver
2	chr2:51518000-51521200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr2:51519600-51520200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr2:51519600-51520200	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr2:51519600-51520400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr2:51519600-51520600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr2:51519600-51521000	Enhancers	HUES48 Cell Line	embryonic stem cell

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