Variant report

Variant	rs2861691
Chromosome Location	chr2:67838694-67838695
allele	C/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:36)

rs_ID	r²[population]
rs10196304	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10490723	0.92[ASN][1000 genomes]
rs12477088	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12618268	0.90[ASN][1000 genomes]
rs12987509	0.89[ASN][1000 genomes]
rs12989021	0.88[ASN][1000 genomes]
rs12992403	0.92[ASN][1000 genomes]
rs12997331	0.89[ASN][1000 genomes]
rs13003698	0.87[ASN][1000 genomes]
rs13005138	0.88[ASN][1000 genomes]
rs13013880	0.89[ASN][1000 genomes]
rs13019532	0.89[ASN][1000 genomes]
rs13021903	0.92[ASN][1000 genomes]
rs13023342	0.88[ASN][1000 genomes]
rs13025342	0.90[ASN][1000 genomes]
rs13025376	0.93[ASN][1000 genomes]
rs13028371	0.91[ASN][1000 genomes]
rs17033996	0.87[ASN][1000 genomes]
rs2861683	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2861685	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34724856	0.85[ASN][1000 genomes]
rs35002785	0.90[ASN][1000 genomes]
rs35179846	0.95[ASN][1000 genomes]
rs35820615	0.90[ASN][1000 genomes]
rs4362542	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4465757	0.81[ASN][1000 genomes]
rs4542832	0.84[ASN][1000 genomes]
rs62156279	0.90[ASN][1000 genomes]
rs6546315	0.89[ASN][1000 genomes]
rs6546319	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6731513	0.92[ASN][1000 genomes]
rs6732490	0.86[ASN][1000 genomes]
rs6746168	0.83[ASN][1000 genomes]
rs6756226	0.85[ASN][1000 genomes]
rs6760893	0.86[ASN][1000 genomes]
rs980226	0.87[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534389	chr2:67388428-68225338	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67828000-67839400	Weak transcription	Placenta	Placenta

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