Variant report

Variant	rs61938117
Chromosome Location	chr12:119923456-119923457
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11064799	0.93[EUR][1000 genomes]
rs12099618	0.92[EUR][1000 genomes]
rs12297032	0.93[EUR][1000 genomes]
rs12297270	0.93[EUR][1000 genomes]
rs12322169	0.93[EUR][1000 genomes]
rs12322291	0.93[EUR][1000 genomes]
rs1464374	1.00[EUR][1000 genomes]
rs17404345	0.82[AMR][1000 genomes]
rs17482376	0.82[AMR][1000 genomes]
rs2293495	0.93[EUR][1000 genomes]
rs4767822	0.82[AMR][1000 genomes]
rs61938079	0.85[EUR][1000 genomes]
rs61938109	0.93[EUR][1000 genomes]
rs61938115	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7304132	0.81[EUR][1000 genomes]
rs7967638	0.93[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	nsv1047036	chr12:119477583-119992640	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv916688	chr12:119801814-120044407	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv832529	chr12:119863378-120071646	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr12:119917400-119924600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr12:119921000-119924600	Weak transcription	Spleen	Spleen

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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