Variant report

Variant	rs12215967
Chromosome Location	chr6:55314245-55314246
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:55313713..55314676-chr6:55750196..55751674,4	MCF-7	breast:
2	chr6:55314098..55314636-chr6:55750998..55751586,2	MCF-7	breast:
3	chr6:55313873..55314721-chr6:55806208..55806737,2	MCF-7	breast:
4	chr6:55313762..55314282-chr6:56157199..56157825,2	MCF-7	breast:
5	chr6:55313718..55314729-chr6:55817986..55818869,4	MCF-7	breast:
6	chr6:55313181..55315342-chr6:55800874..55802800,2	MCF-7	breast:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10456714	0.89[ASN][1000 genomes]
rs10948923	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12191691	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12192987	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12195448	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12195626	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12196586	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12196868	0.80[ASN][1000 genomes]
rs12200360	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12204776	0.91[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12205981	0.91[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12206196	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12206446	0.93[ASN][1000 genomes]
rs12210510	0.91[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12212707	0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12215544	0.87[ASN][1000 genomes]
rs12216528	0.82[ASN][1000 genomes]
rs4236131	0.98[ASN][1000 genomes]
rs4339457	0.91[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs4520003	0.82[ASN][1000 genomes]
rs4712104	0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs62405366	0.87[ASN][1000 genomes]
rs62405367	0.87[ASN][1000 genomes]
rs62405368	0.87[ASN][1000 genomes]
rs62405400	0.81[ASN][1000 genomes]
rs7762185	0.87[ASN][1000 genomes]
rs9382502	0.82[ASN][1000 genomes]
rs9396103	0.82[ASN][1000 genomes]
rs9464263	0.82[ASN][1000 genomes]
rs9475343	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv885903	chr6:55142337-55344782	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv885904	chr6:55156812-55344782	Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1034037	chr6:55222409-56069600	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv470819	chr6:55236937-55368815	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1031179	chr6:55237283-55372905	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1029436	chr6:55237283-55386038	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1028560	chr6:55237723-55378113	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1024550	chr6:55237723-55387481	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv462948	chr6:55238091-55368815	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv603163	chr6:55238091-55368815	Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv1018622	chr6:55297854-55320311	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:55310600-55315000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr6:55312400-55315400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr6:55313600-55315200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:55313600-55317800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr6:55313800-55314400	Enhancers	Fetal Lung	lung
6	chr6:55314000-55314600	Enhancers	Adipose Nuclei	Adipose
7	chr6:55314200-55316400	Weak transcription	Fetal Heart	heart

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