Variant report

Variant	rs72981969
Chromosome Location	chr11:106436758-106436759
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs12418838	1.00[ASN][1000 genomes]
rs12419060	1.00[ASN][1000 genomes]
rs12421832	1.00[ASN][1000 genomes]
rs12805720	1.00[ASN][1000 genomes]
rs17562446	1.00[ASN][1000 genomes]
rs1938614	1.00[ASN][1000 genomes]
rs35704768	1.00[ASN][1000 genomes]
rs72981962	1.00[ASN][1000 genomes]
rs72981984	1.00[ASN][1000 genomes]
rs72981986	1.00[ASN][1000 genomes]
rs72981991	1.00[ASN][1000 genomes]
rs72981994	1.00[ASN][1000 genomes]
rs72983825	1.00[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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106424400-106437000	Weak transcription	Pancreas	Pancrea
2	chr11:106435400-106437600	Enhancers	Dnd41	blood

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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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