Variant report

Variant	rs73185501
Chromosome Location	chr7:103676335-103676336
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10240408	0.82[ASN][1000 genomes]
rs10240682	0.82[ASN][1000 genomes]
rs10255340	0.82[ASN][1000 genomes]
rs10256884	0.98[ASN][1000 genomes]
rs10261266	0.98[ASN][1000 genomes]
rs10480652	0.98[ASN][1000 genomes]
rs10953402	0.97[ASN][1000 genomes]
rs11971200	0.97[ASN][1000 genomes]
rs12536622	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12539921	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17158452	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17158464	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1858811	0.82[ASN][1000 genomes]
rs1858812	1.00[ASN][1000 genomes]
rs1858813	0.86[AFR][1000 genomes]
rs194845	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs194860	0.81[AMR][1000 genomes]
rs4727586	0.89[ASN][1000 genomes]
rs4729945	0.82[ASN][1000 genomes]
rs4729946	0.82[ASN][1000 genomes]
rs4729947	0.82[ASN][1000 genomes]
rs4729948	0.98[ASN][1000 genomes]
rs4729950	0.98[ASN][1000 genomes]
rs4729951	0.98[ASN][1000 genomes]
rs4729952	0.98[ASN][1000 genomes]
rs4729953	0.98[ASN][1000 genomes]
rs4729954	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4729955	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4729956	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4729962	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs56022599	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56325675	0.97[ASN][1000 genomes]
rs58765880	0.82[ASN][1000 genomes]
rs59700255	0.90[EUR][1000 genomes]
rs60297107	0.97[ASN][1000 genomes]
rs66797006	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs66918163	0.82[ASN][1000 genomes]
rs67580058	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73187416	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73189312	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73713263	0.85[AFR][1000 genomes]
rs756742	0.80[ASN][1000 genomes]
rs756744	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv888924	chr7:103637906-103706936	Enhancers Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1018253	chr7:103669491-103731850	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103675800-103676600	Enhancers	K562	blood
2	chr7:103676000-103679600	Enhancers	HepG2	liver

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