Variant report

Variant	rs7994977
Chromosome Location	chr13:62768290-62768291
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs2034288	0.83[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs308614	0.81[ASN][1000 genomes]
rs308615	0.81[ASN][1000 genomes]
rs308616	0.80[ASN][1000 genomes]
rs308618	0.80[ASN][1000 genomes]
rs308619	0.80[ASN][1000 genomes]
rs308620	0.80[ASN][1000 genomes]
rs308622	0.80[ASN][1000 genomes]
rs308623	0.80[ASN][1000 genomes]
rs308624	0.80[ASN][1000 genomes]
rs308627	0.80[ASN][1000 genomes]
rs5020678	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs5020679	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs5020680	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs5020681	0.86[ASN][1000 genomes]
rs66824322	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs7320109	0.87[ASN][1000 genomes]
rs7320115	0.87[ASN][1000 genomes]
rs7981757	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs7982438	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs7982706	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs7983039	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs7983391	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs7987611	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs7988008	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs7989138	0.87[ASN][1000 genomes]
rs7994456	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs8001256	0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs9285236	0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs9317229	0.85[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs9528477	0.87[ASN][1000 genomes]
rs9528478	0.87[ASN][1000 genomes]
rs9528494	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs9528495	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs9528496	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs9528497	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs9528498	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs9528499	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs9539442	0.87[ASN][1000 genomes]
rs9539443	0.87[ASN][1000 genomes]
rs9539452	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs9539453	0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs9539454	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs9539455	0.85[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs9539456	0.86[AFR][1000 genomes];0.87[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	nsv948810	chr13:62003256-62968196	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv832630	chr13:62651865-62811428	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 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	chr13:62768000-62768800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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