Variant report

Variant	rs12190982
Chromosome Location	chr6:54654952-54654953
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10456175	0.82[EUR][1000 genomes]
rs10948858	0.82[EUR][1000 genomes]
rs12195610	0.82[EUR][1000 genomes]
rs12196417	0.82[EUR][1000 genomes]
rs12196807	0.94[EUR][1000 genomes]
rs12197945	0.82[EUR][1000 genomes]
rs12198000	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12198696	0.82[EUR][1000 genomes]
rs12199020	0.89[EUR][1000 genomes]
rs12203906	0.82[EUR][1000 genomes]
rs12203996	0.82[EUR][1000 genomes]
rs12204479	0.82[EUR][1000 genomes]
rs12205707	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12209581	0.82[EUR][1000 genomes]
rs12211620	0.88[EUR][1000 genomes]
rs12215996	0.82[EUR][1000 genomes]
rs12216148	0.82[EUR][1000 genomes]
rs12216154	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12216371	0.82[EUR][1000 genomes]
rs28819710	0.82[EUR][1000 genomes]
rs3913635	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6904875	0.82[EUR][1000 genomes]
rs6915978	0.82[EUR][1000 genomes]
rs72955751	0.82[EUR][1000 genomes]
rs72955777	0.82[EUR][1000 genomes]
rs72955781	0.82[EUR][1000 genomes]
rs72955782	0.82[EUR][1000 genomes]
rs72957545	0.82[EUR][1000 genomes]
rs72957569	0.82[EUR][1000 genomes]
rs72957574	0.82[EUR][1000 genomes]
rs72967427	0.89[EUR][1000 genomes]
rs7745529	0.82[EUR][1000 genomes]
rs7745648	0.82[EUR][1000 genomes]
rs9464136	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9474995	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9475003	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9475012	0.82[EUR][1000 genomes]
rs9475022	0.82[EUR][1000 genomes]
rs9475023	0.82[EUR][1000 genomes]
rs9475025	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv885900	chr6:54517968-54852462	Active TSS Bivalent Enhancer Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv885902	chr6:54588069-54656673	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv437968	chr6:54651356-54660245	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:54653200-54667800	Weak transcription	Placenta Amnion	Placenta Amnion

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