Variant report

Variant	rs62442621
Chromosome Location	chr7:38732657-38732658
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10499611	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17150906	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17171446	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17171473	0.88[AMR][1000 genomes]
rs62442053	1.00[AMR][1000 genomes]
rs62442615	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62442618	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62442619	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs62442622	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62444122	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62444124	1.00[AMR][1000 genomes];0.92[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	nsv887965	chr7:38706384-38793243	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr7:38722200-38733800	Weak transcription	Right Atrium	heart
2	chr7:38732600-38733200	Enhancers	Primary hematopoietic stem cells	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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