Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1146883	0.85[ASN][1000 genomes]
rs1146888	0.84[ASN][1000 genomes]
rs1505141	0.86[ASN][1000 genomes]
rs1700826	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17066099	0.94[ASN][1000 genomes]
rs1757889	0.91[EUR][1000 genomes]
rs1847629	0.91[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs1929731	0.84[ASN][1000 genomes]
rs2657128	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2777732	0.85[ASN][1000 genomes]
rs4142608	0.93[ASN][1000 genomes]
rs4142610	0.94[ASN][1000 genomes]
rs61963409	0.94[ASN][1000 genomes]
rs8001163	0.94[ASN][1000 genomes]
rs924894	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs924895	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9318421	0.92[ASN][1000 genomes]
rs9530536	0.94[ASN][1000 genomes]
rs9544243	0.85[ASN][1000 genomes]
rs9544244	0.85[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	nsv1044736	chr13:76728655-77066435	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76899200-76911400	Weak transcription	Aorta	Aorta
2	chr13:76899600-76905000	Weak transcription	Colon Smooth Muscle	Colon
3	chr13:76902800-76905800	Enhancers	Fetal Stomach	stomach
4	chr13:76903800-76906400	Enhancers	Rectal Smooth Muscle	rectum
5	chr13:76904000-76904200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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