Variant report

Variant	rs2890615
Chromosome Location	chr2:142302920-142302921
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs11681928	1.00[CHB][hapmap]
rs11902974	1.00[YRI][hapmap];0.80[AFR][1000 genomes]
rs12467062	0.95[CEU][hapmap];0.82[JPT][hapmap];0.90[EUR][1000 genomes]
rs12468830	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12469217	0.96[ASN][1000 genomes]
rs12470072	1.00[CHB][hapmap];0.85[EUR][1000 genomes]
rs12470665	0.86[JPT][hapmap]
rs12476668	0.84[EUR][1000 genomes]
rs12476844	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12477753	0.85[JPT][hapmap]
rs12478973	0.91[CEU][hapmap];0.91[JPT][hapmap];0.90[EUR][1000 genomes]
rs12612624	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs12615716	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12615851	0.91[CHB][hapmap]
rs12621499	0.91[CEU][hapmap];0.82[JPT][hapmap];0.85[EUR][1000 genomes]
rs13030335	0.95[JPT][hapmap]
rs13031144	1.00[JPT][hapmap]
rs1483141	0.82[JPT][hapmap]
rs16846426	0.88[YRI][hapmap]
rs16846467	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16846484	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16846506	0.83[CHB][hapmap]
rs16846521	0.95[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs16846522	0.96[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs16846530	0.84[CEU][hapmap];0.95[CHB][hapmap]
rs2170668	0.87[CEU][hapmap];1.00[CHB][hapmap]
rs2200192	0.88[CEU][hapmap];0.87[JPT][hapmap]
rs2381190	0.91[CEU][hapmap];1.00[CHB][hapmap]
rs4384715	0.82[JPT][hapmap]
rs4544370	0.82[JPT][hapmap]
rs4574055	1.00[JPT][hapmap]
rs57933129	0.96[ASN][1000 genomes]
rs6429903	0.82[EUR][1000 genomes]
rs6429908	1.00[CHB][hapmap];0.95[JPT][hapmap]
rs6745610	0.84[YRI][hapmap]
rs72852491	0.84[EUR][1000 genomes]
rs72853570	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72855407	0.95[ASN][1000 genomes]
rs72855428	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7562751	0.91[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs7588818	0.86[JPT][hapmap]
rs7589997	0.85[EUR][1000 genomes]
rs7593962	0.86[JPT][hapmap]
rs7597633	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv583203	chr2:142055133-142378975	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv875240	chr2:142199421-142347455	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
3	nsv834393	chr2:142256714-142431564	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	n/a
4	nsv583212	chr2:142263979-142309330	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
5	nsv459640	chr2:142291211-142345574	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
6	nsv583213	chr2:142291211-142345574	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv583214	chr2:142299923-142458316	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

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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