Variant report

Variant	rs61270372
Chromosome Location	chr3:78882509-78882510
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs12330873	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs167944	1.00[ASN][1000 genomes]
rs28493625	1.00[EUR][1000 genomes]
rs28722753	1.00[EUR][1000 genomes]
rs331133	1.00[ASN][1000 genomes]
rs333501	1.00[ASN][1000 genomes]
rs57657065	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61490942	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6788270	1.00[EUR][1000 genomes]
rs72894427	0.85[AMR][1000 genomes]
rs72894434	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72894439	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72894449	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72894451	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72894453	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72894457	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72894459	0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72894460	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72894461	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72894463	1.00[ASN][1000 genomes]
rs72894464	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72894467	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72894471	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72894474	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72894482	0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72894501	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72896405	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72896408	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72896421	1.00[EUR][1000 genomes]
rs72896425	1.00[EUR][1000 genomes]
rs72896439	1.00[EUR][1000 genomes]
rs72896443	1.00[EUR][1000 genomes]
rs72896444	1.00[EUR][1000 genomes]
rs72896497	1.00[EUR][1000 genomes]
rs72904252	1.00[EUR][1000 genomes]
rs72904254	1.00[EUR][1000 genomes]
rs72904257	1.00[EUR][1000 genomes]
rs72904261	1.00[EUR][1000 genomes]
rs72906145	1.00[EUR][1000 genomes]
rs9808917	1.00[EUR][1000 genomes]
rs9813971	1.00[EUR][1000 genomes]
rs9817408	1.00[EUR][1000 genomes]
rs9818374	1.00[EUR][1000 genomes]
rs9831603	1.00[EUR][1000 genomes]
rs9847098	1.00[EUR][1000 genomes]
rs9872429	1.00[EUR][1000 genomes]
rs9876641	1.00[EUR][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	nsv1010804	chr3:78739648-79087470	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv533681	chr3:78750924-79017336	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:78873200-78888800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:78875600-78884400	Weak transcription	NHDF-Ad	bronchial
3	chr3:78875600-78888800	Weak transcription	Fetal Lung	lung
4	chr3:78879800-78882800	Weak transcription	Brain Substantia Nigra	brain
5	chr3:78882000-78894800	Weak transcription	Fetal Intestine Small	intestine
6	chr3:78882400-78882600	Flanking Active TSS	HepG2	liver

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