Variant report

Variant	rs73370529
Chromosome Location	chr7:79526722-79526723
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:79522831..79524526-chr7:79524961..79527808,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1005245	0.84[EUR][1000 genomes]
rs11975054	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11975127	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12112743	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12113482	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12531118	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12531172	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12531185	0.87[EUR][1000 genomes]
rs12533720	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12539252	0.89[EUR][1000 genomes]
rs17204415	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17204926	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17207519	1.00[EUR][1000 genomes]
rs17793556	0.95[EUR][1000 genomes]
rs17793605	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17793671	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17799797	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2107408	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs55653798	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55698421	0.87[EUR][1000 genomes]
rs55718558	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs56036430	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56107852	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56306195	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56349627	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57609264	0.95[EUR][1000 genomes]
rs59333025	0.80[AMR][1000 genomes]
rs6946316	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6949163	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6949761	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6954060	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6957059	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6957093	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73368692	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs73370544	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73370545	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73370570	1.00[EUR][1000 genomes]
rs73383049	0.89[EUR][1000 genomes]
rs73707160	0.95[EUR][1000 genomes]
rs73709915	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73709922	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73709923	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7783110	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9785059	0.90[AMR][1000 genomes];1.00[EUR][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	nsv888522	chr7:79402551-79619012	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	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	chr7:79526600-79527800	Enhancers	Pancreatic Islets	Pancreatic Islet

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