Variant report

Variant	rs7661156
Chromosome Location	chr4:125355040-125355041
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:125255585..125257138-chr4:125353670..125355565,2	MCF-7	breast:
2	chr4:125353257..125355602-chr4:125631659..125634824,5	MCF-7	breast:
3	chr4:125351638..125355658-chr4:125628330..125634892,8	MCF-7	breast:

Variant related genes	Relation type
ENSG00000151458	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11098750	0.97[ASN][1000 genomes]
rs11098751	0.97[ASN][1000 genomes]
rs17008132	1.00[ASN][1000 genomes]
rs17008138	1.00[ASN][1000 genomes]
rs17008148	0.95[ASN][1000 genomes]
rs17008161	1.00[ASN][1000 genomes]
rs1994809	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2390686	0.91[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.98[MKK][hapmap];0.94[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55779229	0.97[ASN][1000 genomes]
rs72676695	0.92[ASN][1000 genomes]
rs72678414	0.97[ASN][1000 genomes]
rs72678423	0.97[ASN][1000 genomes]
rs72678424	0.97[ASN][1000 genomes]
rs72678453	1.00[ASN][1000 genomes]
rs72678455	1.00[ASN][1000 genomes]
rs72678461	1.00[ASN][1000 genomes]
rs72678463	1.00[ASN][1000 genomes]
rs72678465	0.97[ASN][1000 genomes]
rs72678468	1.00[ASN][1000 genomes]
rs72678469	1.00[ASN][1000 genomes]
rs72678470	1.00[ASN][1000 genomes]
rs72678481	1.00[ASN][1000 genomes]
rs7674379	1.00[ASN][1000 genomes]
rs7692715	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv868977	chr4:124841128-125550637	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv432624	chr4:125013395-125367740	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv998024	chr4:125019384-125380876	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv537241	chr4:125019384-125380876	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1015049	chr4:125037090-125393067	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv879880	chr4:125174817-125494547	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	esv2760890	chr4:125273456-125466931	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv879881	chr4:125280852-125448288	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:125350600-125358800	Weak transcription	Fetal Intestine Small	intestine
2	chr4:125350800-125357000	Weak transcription	Pancreas	Pancrea
3	chr4:125350800-125357200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:125350800-125359000	Weak transcription	Right Atrium	heart
5	chr4:125352400-125356000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:125353800-125357000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr4:125353800-125358800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:125354400-125356200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr4:125354400-125358800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr4:125354400-125359000	Weak transcription	Stomach Mucosa	stomach
11	chr4:125354600-125356200	Weak transcription	Fetal Lung	lung
12	chr4:125354600-125358800	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr4:125354600-125358800	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr4:125354600-125358800	Weak transcription	NHEK	skin
15	chr4:125354800-125356600	Flanking Active TSS	HUVEC	blood vessel
16	chr4:125355000-125357400	Weak transcription	Gastric	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links