Variant report

Variant	rs2624070
Chromosome Location	chr8:3549936-3549937
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 111 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs10089138	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs10095166	0.82[CEU][hapmap];1.00[CHB][hapmap]
rs10104318	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10105577	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs10105599	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs10110793	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs11775478	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11775483	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11778221	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11783239	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12542452	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12542951	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs12544198	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12544795	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs12549735	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13250019	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs13250917	1.00[CHB][hapmap]
rs13275720	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1481706	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs1482197	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1482198	0.85[CEU][hapmap]
rs1482199	0.85[CEU][hapmap]
rs1482200	0.85[CEU][hapmap]
rs17066731	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17067079	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17067268	1.00[CHB][hapmap]
rs1905025	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2251848	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2251850	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2251857	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2449188	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2449207	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2449208	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs2469377	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2469378	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2623581	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2623582	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2623584	0.85[CEU][hapmap]
rs2623585	0.85[CEU][hapmap]
rs2623587	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs2623592	1.00[CHB][hapmap]
rs2623594	0.85[CEU][hapmap];0.81[GIH][hapmap]
rs2623595	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs2623597	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2623606	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2623704	1.00[CHB][hapmap]
rs2623705	1.00[CHB][hapmap]
rs2623706	1.00[CHB][hapmap]
rs2623709	1.00[CHB][hapmap]
rs2623711	1.00[CHB][hapmap]
rs2623712	1.00[CHB][hapmap]
rs2624058	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs2624059	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs2624063	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2624067	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2624068	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2624075	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2624092	0.85[CEU][hapmap]
rs2624094	0.85[CEU][hapmap]
rs2624108	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs2624111	0.85[CEU][hapmap]
rs2720824	1.00[CHB][hapmap]
rs2720830	1.00[CHB][hapmap]
rs2720831	1.00[CHB][hapmap]
rs2720834	1.00[CHB][hapmap]
rs2720836	1.00[CHB][hapmap]
rs4472537	1.00[CHB][hapmap]
rs4503122	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4875776	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs5003043	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs62474723	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6981596	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs6981931	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6983298	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6983391	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6985082	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6994482	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6994494	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.80[GIH][hapmap];1.00[JPT][hapmap]
rs6994669	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs6995848	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6996329	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7015253	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7825205	1.00[CHB][hapmap]
rs7826851	1.00[CHB][hapmap]
rs878488	0.82[CEU][hapmap]
rs900219	0.85[CEU][hapmap]
rs900222	0.85[CEU][hapmap]
rs900223	0.85[CEU][hapmap]
rs900224	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];1.00[JPT][hapmap]
rs9285037	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9285038	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs931204	0.85[CEU][hapmap]
rs9657366	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9792136	1.00[JPT][hapmap]
rs9942728	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9987389	0.85[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025209	chr8:3067655-3754882	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1026998	chr8:3102679-3593264	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1034076	chr8:3168033-3989947	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv539351	chr8:3168033-3989947	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1017164	chr8:3174168-4026811	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv539352	chr8:3174168-4026811	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1018218	chr8:3180287-4089011	Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv1028926	chr8:3318340-3667389	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
9	nsv539353	chr8:3318340-3667389	Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
10	nsv831211	chr8:3504660-3660294	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
11	nsv1017752	chr8:3530971-3754478	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
12	nsv539355	chr8:3530971-3754478	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
13	nsv1025204	chr8:3542586-3889592	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
14	nsv539356	chr8:3542586-3889592	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
15	esv3357414	chr8:3549344-3553542	Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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