Variant report

Variant	rs11629380
Chromosome Location	chr14:84419624-84419625
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10484122	0.82[AMR][1000 genomes]
rs11159625	0.82[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12431590	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12434759	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12435187	0.81[AMR][1000 genomes]
rs12435245	0.82[AMR][1000 genomes]
rs12897738	0.82[AMR][1000 genomes]
rs1547466	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17647821	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs17726697	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs34708795	0.82[AMR][1000 genomes]
rs61985922	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs61985923	0.86[ASN][1000 genomes]
rs61987170	0.86[ASN][1000 genomes]
rs7157753	0.84[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs8003423	0.82[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv902159	chr14:84336944-84447356	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1039271	chr14:84405561-84467550	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:84419000-84436000	Weak transcription	Pancreas	Pancrea

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

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