Variant report

Variant	rs12477753
Chromosome Location	chr2:142331002-142331003
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs12467062	1.00[CHB][hapmap];0.84[JPT][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12468830	0.84[JPT][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12469217	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs12476844	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12478973	1.00[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12615716	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12621499	1.00[CHB][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13031144	0.85[JPT][hapmap]
rs1483141	1.00[CHB][hapmap];0.84[JPT][hapmap]
rs16846467	0.83[JPT][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16846484	0.85[JPT][hapmap];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16846521	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs16846522	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2200192	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2890615	0.85[JPT][hapmap]
rs4363973	0.83[CHB][hapmap]
rs4384715	0.84[JPT][hapmap]
rs4544370	0.84[JPT][hapmap]
rs4574055	0.85[JPT][hapmap]
rs57933129	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs6429908	1.00[YRI][hapmap]
rs72853570	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72855407	0.93[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs72855428	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7557786	0.83[CHB][hapmap]
rs7562751	0.85[JPT][hapmap]
rs7589997	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7593962	1.00[CHB][hapmap];0.84[JPT][hapmap];0.82[YRI][hapmap]
rs7597633	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 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	nsv459640	chr2:142291211-142345574	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
5	nsv583213	chr2:142291211-142345574	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a
6	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
7	nsv1011019	chr2:142314999-142430460	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
8	esv1800912	chr2:142324505-142339047	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	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
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