Variant report

Variant	rs7150018
Chromosome Location	chr14:78966066-78966067
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1015964	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10483907	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1122840	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1122841	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1122842	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1122898	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11622820	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11844960	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12588305	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1468743	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2098518	0.86[EUR][1000 genomes]
rs2193670	0.87[EUR][1000 genomes]
rs35810359	0.98[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4903768	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4903776	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4903777	0.87[EUR][1000 genomes]
rs4903779	0.87[EUR][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	esv2760000	chr14:78875607-79173528	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv2758363	chr14:78903610-79173528	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr14:78966000-78966200	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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