Variant report

Variant	rs6710630
Chromosome Location	chr2:125416536-125416537
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10171962	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10202904	0.82[CHB][hapmap]
rs10496638	0.81[CHB][hapmap]
rs11681479	0.82[CHB][hapmap]
rs11684957	0.81[CHB][hapmap]
rs12619819	0.92[CEU][hapmap];0.81[JPT][hapmap];0.82[EUR][1000 genomes]
rs12711689	0.81[CHB][hapmap]
rs12711690	0.81[CHB][hapmap]
rs13008849	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13022965	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13026562	0.82[CHB][hapmap]
rs13033906	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs13385718	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13386176	0.81[CHB][hapmap]
rs13399532	0.81[CHB][hapmap]
rs13413315	0.81[CHB][hapmap]
rs13415836	0.81[CHB][hapmap]
rs13432730	0.82[CHB][hapmap]
rs17011871	0.82[CHB][hapmap]
rs17011873	0.81[CHB][hapmap]
rs17011877	0.81[CHB][hapmap]
rs17392772	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1869500	0.81[CHB][hapmap]
rs35658694	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4848254	0.91[CHB][hapmap];0.87[JPT][hapmap]
rs4848258	0.82[CHB][hapmap]
rs4848963	1.00[CEU][hapmap];0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4848965	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4848966	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6541968	0.82[CHB][hapmap]
rs6739399	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap]
rs721520	0.82[CHB][hapmap]
rs7567761	0.82[CHB][hapmap]
rs7567777	0.81[CHB][hapmap]
rs7568564	0.81[CHB][hapmap]
rs7569075	0.82[CHB][hapmap]
rs7596874	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7597429	0.81[CHB][hapmap]
rs7601415	0.81[CHB][hapmap]
rs936027	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834357	chr2:125258157-125421507	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv834359	chr2:125367872-125536022	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
3	nsv428727	chr2:125372897-125512949	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island	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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chromosomal regions: chr1:12345-34567

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