Variant report

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10112818	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10216383	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11786785	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12545695	0.84[ASN][1000 genomes]
rs12549981	0.86[EUR][1000 genomes]
rs12679386	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13252824	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1385980	0.82[ASN][1000 genomes]
rs1552378	0.84[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs1552379	0.84[ASN][1000 genomes]
rs1552380	0.92[AFR][1000 genomes]
rs17676043	0.94[ASN][1000 genomes]
rs17676077	0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2385548	0.80[ASN][1000 genomes]
rs3812424	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62503966	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6984738	0.83[AFR][1000 genomes]
rs6991925	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7002909	0.83[AFR][1000 genomes]
rs7008449	0.84[ASN][1000 genomes]
rs7388394	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	nsv916355	chrX:92984966-93234497	Enhancers Bivalent Enhancer 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	chrX:93131400-93134600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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