Variant report

Variant	rs58427815
Chromosome Location	chr11:106431323-106431324
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10502073	0.83[ASN][1000 genomes]
rs10895982	0.80[ASN][1000 genomes]
rs11211821	0.94[ASN][1000 genomes]
rs17105845	0.99[ASN][1000 genomes]
rs1791599	0.82[ASN][1000 genomes]
rs1791600	0.82[ASN][1000 genomes]
rs1793067	0.82[ASN][1000 genomes]
rs1793068	0.82[ASN][1000 genomes]
rs1793069	0.80[ASN][1000 genomes]
rs66852810	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72981965	0.97[ASN][1000 genomes]
rs72983814	0.93[ASN][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	nsv1048381	chr11:105945117-106561574	Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 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	chr11:106424400-106437000	Weak transcription	Pancreas	Pancrea

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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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