Variant report

Variant	rs7275576
Chromosome Location	chr21:37964619-37964620
allele	C/T
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:49)

rs_ID	r²[population]
rs11910519	0.89[ASN][1000 genomes]
rs12386295	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12482375	0.89[ASN][1000 genomes]
rs13050224	0.84[ASN][1000 genomes]
rs13050577	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13051386	0.89[ASN][1000 genomes]
rs2032150	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2409822	0.89[ASN][1000 genomes]
rs2734392	0.86[ASN][1000 genomes]
rs2734393	0.86[ASN][1000 genomes]
rs2835394	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2835397	0.92[ASN][1000 genomes]
rs2835399	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2835400	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2845783	0.85[ASN][1000 genomes]
rs2845784	0.86[ASN][1000 genomes]
rs2845785	0.86[ASN][1000 genomes]
rs2845786	0.86[ASN][1000 genomes]
rs2850085	0.86[ASN][1000 genomes]
rs34053958	0.90[ASN][1000 genomes]
rs34521064	0.90[ASN][1000 genomes]
rs382620	0.84[ASN][1000 genomes]
rs386394	0.85[ASN][1000 genomes]
rs386752	0.85[ASN][1000 genomes]
rs390584	0.85[ASN][1000 genomes]
rs400731	0.85[ASN][1000 genomes]
rs405828	0.85[ASN][1000 genomes]
rs412510	0.85[ASN][1000 genomes]
rs419513	0.85[ASN][1000 genomes]
rs420352	0.86[ASN][1000 genomes]
rs420885	0.85[ASN][1000 genomes]
rs426275	0.85[ASN][1000 genomes]
rs430159	0.85[ASN][1000 genomes]
rs431741	0.85[ASN][1000 genomes]
rs432137	0.85[ASN][1000 genomes]
rs432294	0.86[ASN][1000 genomes]
rs432706	0.85[ASN][1000 genomes]
rs4372989	0.89[ASN][1000 genomes]
rs437724	0.85[ASN][1000 genomes]
rs438064	0.86[ASN][1000 genomes]
rs438492	0.85[ASN][1000 genomes]
rs441389	0.85[ASN][1000 genomes]
rs441524	0.85[ASN][1000 genomes]
rs4528850	0.89[ASN][1000 genomes]
rs7280686	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7281637	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs876780	0.85[ASN][1000 genomes]
rs9305597	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9983642	0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834090	chr21:37812545-38009542	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1064290	chr21:37878964-37983133	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr21:37955400-37965400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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