Variant report

Variant	rs12192131
Chromosome Location	chr6:72298478-72298479
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10485020	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs1076994	1.00[AFR][1000 genomes]
rs10942960	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs12189736	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12194008	1.00[AFR][1000 genomes]
rs12203374	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs12207658	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12209719	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs12210828	1.00[AFR][1000 genomes]
rs12212596	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12212719	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12212834	1.00[AFR][1000 genomes]
rs12214266	0.85[AMR][1000 genomes]
rs12214683	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12214970	0.85[EUR][1000 genomes]
rs12215019	0.85[EUR][1000 genomes]
rs12524994	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12526974	0.85[AMR][1000 genomes]
rs12527016	0.85[AMR][1000 genomes]
rs13196378	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs13205327	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs13220610	0.85[AMR][1000 genomes]
rs17453537	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17550741	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34080587	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35128468	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35240683	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs35345970	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs36088985	1.00[AFR][1000 genomes]
rs3912534	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62404299	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62407670	1.00[AFR][1000 genomes]
rs67651127	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs6902698	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6903314	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6927741	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs71555493	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs7775176	0.85[AMR][1000 genomes]
rs829273	0.82[AMR][1000 genomes];0.86[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	nsv830685	chr6:72244007-72410757	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:72298200-72298600	Active TSS	iPS-15b Cell Line	embryonic stem cell
2	chr6:72298200-72298600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr6:72298200-72298600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:72298200-72298600	Enhancers	Pancreas	Pancrea

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