Variant report

Variant	rs1374793
Chromosome Location	chr3:160638505-160638506
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:160637526..160640415-chr3:160816945..160818993,2	MCF-7	breast:
2	chr3:160471577..160473920-chr3:160637599..160639547,2	MCF-7	breast:
3	chr3:64008871..64009613-chr3:160638456..160639098,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000163590	Chromatin interaction
ENSG00000260572	Chromatin interaction
ENSG00000163636	Chromatin interaction
ENSG00000169255	Chromatin interaction

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs1037888	0.88[CEU][hapmap]
rs10513559	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs10513562	1.00[CEU][hapmap]
rs11708813	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs11716265	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs11922752	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11924510	0.82[AFR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12639128	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13064176	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13071909	0.86[EUR][1000 genomes]
rs13073571	0.87[EUR][1000 genomes]
rs13086250	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13089559	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13092102	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs13097130	0.87[EUR][1000 genomes]
rs13098884	1.00[CEU][hapmap];0.81[EUR][1000 genomes]
rs1447618	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1447619	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1447620	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1610158	0.88[CEU][hapmap]
rs17236725	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17236746	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs17826438	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1839015	0.83[EUR][1000 genomes]
rs1839021	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2121718	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs2306061	0.84[CEU][hapmap]
rs2593812	1.00[CEU][hapmap]
rs34168351	0.85[EUR][1000 genomes]
rs34297047	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4557202	0.84[CEU][hapmap]
rs4679662	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4679666	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4679922	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs4679924	0.96[CEU][hapmap];0.88[EUR][1000 genomes]
rs4679926	1.00[CEU][hapmap]
rs5004752	1.00[CEU][hapmap]
rs55672403	0.80[EUR][1000 genomes]
rs55888276	0.89[EUR][1000 genomes]
rs55956394	0.86[EUR][1000 genomes]
rs56665329	0.86[EUR][1000 genomes]
rs61105146	0.87[EUR][1000 genomes]
rs62270272	0.84[EUR][1000 genomes]
rs62270274	0.87[EUR][1000 genomes]
rs62270275	0.87[EUR][1000 genomes]
rs62280303	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62280331	0.81[EUR][1000 genomes]
rs62280333	0.81[EUR][1000 genomes]
rs6441339	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6441354	0.83[CEU][hapmap]
rs6764019	1.00[CEU][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6796201	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6799160	0.92[CEU][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6804650	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs6806054	1.00[CEU][hapmap]
rs6809177	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs723757	0.90[EUR][1000 genomes]
rs7622047	0.88[CEU][hapmap]
rs7632423	1.00[CEU][hapmap]
rs778642	1.00[CEU][hapmap]
rs778643	1.00[CEU][hapmap]
rs778649	1.00[CEU][hapmap]
rs778653	1.00[CEU][hapmap]
rs778654	1.00[CEU][hapmap]
rs778657	1.00[CEU][hapmap]
rs796609	1.00[CEU][hapmap]
rs898680	0.88[CEU][hapmap]
rs898681	0.88[CEU][hapmap]
rs9290065	0.96[CEU][hapmap]
rs9790132	0.96[CEU][hapmap];0.90[EUR][1000 genomes]
rs980975	0.88[CEU][hapmap]
rs980976	0.88[CEU][hapmap]
rs9811594	1.00[CEU][hapmap]
rs9847866	0.96[CEU][hapmap]
rs9860360	1.00[CEU][hapmap]
rs9875200	1.00[CEU][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532666	chr3:159777847-160703202	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:160630200-160641400	Weak transcription	Psoas Muscle	Psoas
2	chr3:160635400-160644000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr3:160635400-160649200	Weak transcription	Fetal Brain Female	brain
4	chr3:160636000-160644000	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr3:160637400-160638800	Enhancers	Colon Smooth Muscle	Colon
6	chr3:160638200-160639000	Enhancers	Fetal Brain Male	brain
7	chr3:160638200-160641800	Weak transcription	Left Ventricle	heart
8	chr3:160638200-160647200	Weak transcription	Right Ventricle	heart
9	chr3:160638400-160643800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr3:160638400-160643800	Weak transcription	Right Atrium	heart

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