Variant report

Variant	rs657736
Chromosome Location	chr5:111252996-111252997
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1003272	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10515435	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11749310	0.93[ASN][1000 genomes]
rs13360997	0.87[ASN][1000 genomes]
rs17133737	1.00[EUR][1000 genomes]
rs17133745	1.00[EUR][1000 genomes]
rs17133824	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17133845	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17133847	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17133862	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17133873	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17133879	0.85[ASN][1000 genomes]
rs17133882	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17133892	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1864136	0.86[ASN][1000 genomes]
rs506401	1.00[EUR][1000 genomes]
rs56243059	0.83[ASN][1000 genomes]
rs56405886	0.90[ASN][1000 genomes]
rs57227445	0.83[ASN][1000 genomes]
rs57342469	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs575328	1.00[EUR][1000 genomes]
rs58429198	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59874488	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs60095412	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs605747	1.00[EUR][1000 genomes]
rs61169291	0.99[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs641552	1.00[EUR][1000 genomes]
rs649429	0.82[EUR][1000 genomes]
rs6594547	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73787704	0.83[ASN][1000 genomes]
rs73787708	0.84[ASN][1000 genomes]
rs73787719	0.82[ASN][1000 genomes]
rs7701160	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7706739	1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7708380	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7708790	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7719956	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7723663	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7728161	1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7737873	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs967985	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	nsv599367	chr5:110924280-111602713	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 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	chr5:111249200-111256200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:111252800-111254000	Weak transcription	Dnd41	blood

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