Variant report

Variant	rs7975334
Chromosome Location	chr12:20839851-20839852
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs12578492	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1399937	0.88[ASN][1000 genomes]
rs1399938	0.82[ASN][1000 genomes]
rs3794270	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs3809208	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs55661764	0.97[ASN][1000 genomes]
rs57238599	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57312777	1.00[ASN][1000 genomes]
rs59508686	0.97[ASN][1000 genomes]
rs60480171	0.88[ASN][1000 genomes]
rs61579575	0.82[ASN][1000 genomes]
rs61623220	0.88[ASN][1000 genomes]
rs6487131	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs6487132	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs67017312	1.00[ASN][1000 genomes]
rs67028347	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72658759	0.88[ASN][1000 genomes]
rs72658760	1.00[ASN][1000 genomes]
rs72658761	0.88[ASN][1000 genomes]
rs7303066	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs7310399	0.87[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7314545	1.00[CHB][hapmap]
rs73240436	0.97[ASN][1000 genomes]
rs73240439	0.91[ASN][1000 genomes]
rs73240441	0.97[ASN][1000 genomes]
rs74065151	0.88[ASN][1000 genomes]
rs74065172	0.82[ASN][1000 genomes]
rs74065173	0.82[ASN][1000 genomes]
rs7960786	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs7975280	0.88[ASN][1000 genomes]
rs7978760	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1048067	chr12:20363755-20874845	Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv541408	chr12:20363755-20874845	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
3	nsv1043890	chr12:20659151-21309993	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv541410	chr12:20659151-21309993	Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	nsv1054997	chr12:20682009-21292602	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:20816400-20840000	Weak transcription	Right Ventricle	heart
2	chr12:20828600-20840200	Weak transcription	Osteobl	bone
3	chr12:20833200-20840000	Weak transcription	Fetal Intestine Small	intestine
4	chr12:20834200-20842200	Weak transcription	Ovary	ovary
5	chr12:20834200-20846600	Weak transcription	Fetal Stomach	stomach
6	chr12:20834600-20840600	Weak transcription	Left Ventricle	heart
7	chr12:20838800-20849800	Weak transcription	Hela-S3	cervix
8	chr12:20839400-20840000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links