Variant report

Variant	rs1249455
Chromosome Location	chr2:141925075-141925076
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10169082	0.96[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap]
rs10180339	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10189024	0.92[CEU][hapmap];0.86[CHB][hapmap];0.84[CHD][hapmap];0.86[JPT][hapmap];0.86[TSI][hapmap]
rs10194319	1.00[CHB][hapmap];0.87[JPT][hapmap]
rs1033284	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]
rs1249426	0.93[ASW][hapmap];0.96[CEU][hapmap];0.82[CHB][hapmap];0.84[CHD][hapmap];0.83[JPT][hapmap];0.91[TSI][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs1249429	0.87[CEU][hapmap];0.92[JPT][hapmap]
rs1249433	0.93[YRI][hapmap];0.82[AFR][1000 genomes]
rs1249447	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1249448	0.87[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1249452	0.96[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap]
rs1249454	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1249457	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[CHD][hapmap];0.93[JPT][hapmap];0.87[MKK][hapmap];0.93[YRI][hapmap]
rs1249458	0.93[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.93[JPT][hapmap];0.85[MKK][hapmap];0.82[TSI][hapmap];0.93[YRI][hapmap]
rs12613639	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs12691594	0.92[CEU][hapmap];0.83[TSI][hapmap];0.81[EUR][1000 genomes]
rs1518800	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1543181	0.92[CEU][hapmap];0.86[CHB][hapmap];0.83[TSI][hapmap]
rs1714259	0.92[CEU][hapmap];0.91[CHB][hapmap];0.93[JPT][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2203809	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2222232	0.83[EUR][1000 genomes]
rs2222233	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.82[TSI][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6711588	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6730244	0.95[CHB][hapmap];0.83[GIH][hapmap];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6741156	0.87[CHD][hapmap]
rs7583934	0.96[CEU][hapmap];0.87[TSI][hapmap]
rs9287313	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv583198	chr2:141510791-142150620	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv817518	chr2:141714174-142287302	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv875218	chr2:141800473-141925845	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1003799	chr2:141803314-142033675	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv459563	chr2:141803602-141925075	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv583200	chr2:141803602-141925075	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1009434	chr2:141832339-142156180	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv875227	chr2:141841920-141928275	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv875228	chr2:141841920-141949292	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv1005236	chr2:141860005-142047695	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv535948	chr2:141860005-142047695	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv875229	chr2:141905052-141951944	Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	nsv963885	chr2:141918827-141927844	Enhancers	TF binding region Chromatin interactive 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
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