Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10187814	0.90[AMR][1000 genomes]
rs10188019	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10195520	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10205532	0.85[YRI][hapmap];0.82[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs10469964	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11883986	0.90[AMR][1000 genomes]
rs11902280	0.90[AMR][1000 genomes]
rs12105464	0.89[AMR][1000 genomes]
rs13390314	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13391151	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13397183	0.90[AMR][1000 genomes]
rs13399612	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13405937	0.90[AMR][1000 genomes]
rs13416510	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs13426439	0.88[AFR][1000 genomes]
rs28581818	0.90[AMR][1000 genomes]
rs6546784	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6738020	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7563870	0.94[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7585242	0.90[AMR][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	nsv834259	chr2:72941118-73114106	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:73053600-73060000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr2:73057600-73060400	Weak transcription	Placenta	Placenta

Quick Search: