Variant report

Variant	rs57640416
Chromosome Location	chr3:68834978-68834979
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs11128091	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12163576	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13070250	0.81[EUR][1000 genomes]
rs13072126	0.82[ASN][1000 genomes]
rs13087144	0.86[ASN][1000 genomes]
rs13433766	0.86[ASN][1000 genomes]
rs13433979	0.86[ASN][1000 genomes]
rs1489996	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1565384	0.82[EUR][1000 genomes]
rs1565385	0.82[EUR][1000 genomes]
rs17047972	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1813868	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1873264	0.90[ASN][1000 genomes]
rs1873266	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2130438	0.81[EUR][1000 genomes]
rs2171868	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35508315	0.86[ASN][1000 genomes]
rs35994466	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs36038335	0.87[ASN][1000 genomes]
rs4093385	0.87[ASN][1000 genomes]
rs4855505	0.82[EUR][1000 genomes]
rs55691267	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56109105	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs56889723	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs58972171	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59548135	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6773337	0.82[ASN][1000 genomes]
rs72925108	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs72925176	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7612656	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7621862	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7623995	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7647961	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7650449	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs870241	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs931433	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs971092	0.90[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	nsv834722	chr3:68775036-68974120	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 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	chr3:68829800-68844000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:68833400-68837000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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