Variant report

Variant	rs7979155
Chromosome Location	chr12:63720061-63720062
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:63719488..63722157-chr12:63724086..63726677,2	K562	blood:
2	chr12:63714796..63717603-chr12:63718432..63720998,3	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10467073	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10878037	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10878038	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10878043	0.82[ASN][1000 genomes]
rs10878044	0.84[ASN][1000 genomes]
rs11174927	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11174934	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11174940	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11174954	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11174955	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11174957	0.82[ASN][1000 genomes]
rs11174960	0.92[EUR][1000 genomes]
rs11174962	1.00[EUR][1000 genomes]
rs11174963	1.00[EUR][1000 genomes]
rs11174964	1.00[EUR][1000 genomes]
rs11174967	1.00[EUR][1000 genomes]
rs11174968	1.00[EUR][1000 genomes]
rs11174972	1.00[EUR][1000 genomes]
rs11174973	1.00[EUR][1000 genomes]
rs11174974	0.92[EUR][1000 genomes]
rs11174975	1.00[EUR][1000 genomes]
rs11174977	1.00[EUR][1000 genomes]
rs11174986	1.00[EUR][1000 genomes]
rs11175001	1.00[EUR][1000 genomes]
rs1146103	0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1146107	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1146108	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11533671	1.00[EUR][1000 genomes]
rs11534939	1.00[EUR][1000 genomes]
rs12226978	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12229731	1.00[EUR][1000 genomes]
rs12230420	0.92[EUR][1000 genomes]
rs12230481	1.00[EUR][1000 genomes]
rs12231031	0.82[ASN][1000 genomes]
rs12309753	0.82[ASN][1000 genomes]
rs1250658	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1251774	0.82[ASN][1000 genomes]
rs1607802	1.00[EUR][1000 genomes]
rs17099426	1.00[EUR][1000 genomes]
rs73320274	0.82[ASN][1000 genomes]
rs73321936	0.82[ASN][1000 genomes]
rs73321977	1.00[EUR][1000 genomes]
rs7342410	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9805075	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046836	chr12:63392391-64377169	Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
2	nsv1035736	chr12:63526274-63920372	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv541510	chr12:63526274-63920372	Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1052866	chr12:63562442-63879794	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv541511	chr12:63562442-63879794	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv832438	chr12:63571652-63745827	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv832439	chr12:63688083-63865226	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:63718800-63720600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links