Variant report

Variant	rs6732308
Chromosome Location	chr2:182996188-182996189
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:182754700..182758987-chr2:182995578..182999206,6	MCF-7	breast:
2	chr2:182940136..182945901-chr2:182990915..182998605,17	MCF-7	breast:
3	chr2:182942463..182945440-chr2:182995161..182998579,4	MCF-7	breast:
4	chr2:182759435..182761686-chr2:182994619..182996651,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000138434	Chromatin interaction
ENSG00000260742	Chromatin interaction

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10181222	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10181420	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10193834	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10197864	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10205020	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10451546	0.87[EUR][1000 genomes]
rs10930990	0.88[AFR][1000 genomes]
rs11686047	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11694699	0.80[EUR][1000 genomes]
rs11899083	0.97[EUR][1000 genomes]
rs12473915	0.92[EUR][1000 genomes]
rs12474446	0.96[EUR][1000 genomes]
rs13398100	0.96[EUR][1000 genomes]
rs1400003	0.86[EUR][1000 genomes]
rs1400004	0.86[EUR][1000 genomes]
rs1432524	0.96[EUR][1000 genomes]
rs1515897	0.96[EUR][1000 genomes]
rs16822592	0.97[EUR][1000 genomes]
rs17648960	0.97[EUR][1000 genomes]
rs1878093	0.97[EUR][1000 genomes]
rs1882212	0.87[EUR][1000 genomes]
rs1921149	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1921150	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1921151	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1921152	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2163697	0.97[EUR][1000 genomes]
rs2195879	0.97[EUR][1000 genomes]
rs3731689	0.97[EUR][1000 genomes]
rs4666813	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4666814	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60286884	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6433954	0.97[EUR][1000 genomes]
rs6744499	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6748404	0.87[EUR][1000 genomes]
rs6760627	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6760977	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73040730	0.97[EUR][1000 genomes]
rs7558141	0.97[EUR][1000 genomes]
rs7558159	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7558558	0.87[EUR][1000 genomes]
rs7567207	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7593639	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7593912	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7606356	0.97[EUR][1000 genomes]
rs768742	0.96[EUR][1000 genomes]
rs9288078	0.86[EUR][1000 genomes]
rs953267	0.87[EUR][1000 genomes]
rs998617	0.87[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	nsv875477	chr2:182938377-183086478	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv875478	chr2:182960289-182998122	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:182966800-182996400	Weak transcription	Fetal Thymus	thymus
2	chr2:182993800-182996400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr2:182994000-182996400	Weak transcription	Aorta	Aorta
4	chr2:182994400-182996800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr2:182994600-182996400	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr2:182994600-182996400	Weak transcription	Osteobl	bone
7	chr2:182994600-182996600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr2:182995200-182996600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr2:182995400-182996600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr2:182995600-182996800	Weak transcription	Hela-S3	cervix
11	chr2:182995600-182997800	Weak transcription	HMEC	breast
12	chr2:182995800-182996800	Weak transcription	Fetal Kidney	kidney

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