Variant report

Variant	rs62137450
Chromosome Location	chr2:49085249-49085250
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs4254550	0.83[AFR][1000 genomes]
rs4481040	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56963902	1.00[EUR][1000 genomes]
rs62137362	0.86[EUR][1000 genomes]
rs62137363	0.86[EUR][1000 genomes]
rs62137365	0.86[EUR][1000 genomes]
rs62137368	0.86[EUR][1000 genomes]
rs62137393	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62137394	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62137396	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62137397	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62137399	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62137400	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62137402	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62137403	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62137444	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62137445	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62137449	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62137451	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62137452	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62137454	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62161788	0.86[EUR][1000 genomes]
rs62161789	0.80[EUR][1000 genomes]
rs72884590	0.86[EUR][1000 genomes]
rs72886209	0.85[EUR][1000 genomes]
rs72889120	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002793	chr2:48771220-49466550	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1004965	chr2:48796170-49443587	Bivalent Enhancer Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv535684	chr2:48796170-49443587	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv498119	chr2:48808834-49422647	Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
5	nsv998864	chr2:49015878-49230000	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr2:49081800-49085800	Enhancers	Ovary	ovary
2	chr2:49084800-49085600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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