Variant report

Variant	rs61940763
Chromosome Location	chr12:48851637-48851638
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs11168613	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12578360	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12579133	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12580859	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12581223	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12582586	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12582594	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs17234937	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28889727	0.80[ASN][1000 genomes]
rs4397895	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4426170	0.82[EUR][1000 genomes]
rs4485148	0.87[AFR][1000 genomes]
rs4547144	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55647233	0.80[ASN][1000 genomes]
rs55667337	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55685217	0.80[ASN][1000 genomes]
rs55971664	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs55983865	0.97[EUR][1000 genomes]
rs56034252	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56191575	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs59325389	0.87[AFR][1000 genomes]
rs59337124	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs61940764	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61940766	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61940767	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61940768	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61940776	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61940777	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61940779	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61940780	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61940822	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61942782	0.87[AFR][1000 genomes]
rs61942783	0.87[AFR][1000 genomes]
rs61942784	0.87[AFR][1000 genomes]
rs61942785	1.00[AFR][1000 genomes]
rs61942786	0.80[ASN][1000 genomes]
rs61942812	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs61942813	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs61942816	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs61942817	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs61942828	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61942829	0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61942830	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs61942831	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][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	nsv427911	chr12:48670336-48979396	Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
2	nsv977157	chr12:48839854-48852791	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region lncRNA	3 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	chr12:48851600-48851800	Enhancers	Brain Angular Gyrus	brain
2	chr12:48851600-48851800	Enhancers	Pancreas	Pancrea

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