Variant report

Variant	rs7311320
Chromosome Location	chr12:46688564-46688565
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]
rs56818305	0.85[AFR][1000 genomes]
rs58015896	0.85[AFR][1000 genomes]
rs59268437	0.90[AFR][1000 genomes]
rs74081917	0.95[AFR][1000 genomes]
rs74081935	0.85[AFR][1000 genomes]
rs74081980	0.85[AFR][1000 genomes]
rs74081983	0.85[AFR][1000 genomes]
rs74081996	0.90[AFR][1000 genomes]
rs74082091	1.00[AFR][1000 genomes]
rs74082100	1.00[AFR][1000 genomes]
rs74084027	1.00[AFR][1000 genomes]
rs74084032	0.90[AFR][1000 genomes]
rs7965500	1.00[AFR][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	nsv832398	chr12:46611692-46825530	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	181 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	chr12:46688400-46690600	Weak transcription	Primary B cells from cord blood	blood

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

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