Variant report

Variant	rs615165
Chromosome Location	chr4:119181163-119181164
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:119180318..119182171-chr4:119183748..119185838,2	MCF-7	breast:
2	chr4:119178183..119181452-chr4:119198246..119201177,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000269893	Chromatin interaction

Extended variants
information (count: 130 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:121)

rs_ID	r²[population]
rs10000812	0.83[ASN][1000 genomes]
rs10008049	0.82[ASN][1000 genomes]
rs10014096	0.81[ASN][1000 genomes]
rs10015232	0.82[ASN][1000 genomes]
rs10016285	0.82[ASN][1000 genomes]
rs10021781	0.82[ASN][1000 genomes]
rs10023699	0.82[ASN][1000 genomes]
rs10033412	0.81[ASN][1000 genomes]
rs1022287	0.81[ASN][1000 genomes]
rs1022288	0.82[ASN][1000 genomes]
rs10440400	0.82[ASN][1000 genomes]
rs11098427	0.82[ASN][1000 genomes]
rs11098428	0.82[ASN][1000 genomes]
rs11728724	0.81[ASN][1000 genomes]
rs11937777	0.81[ASN][1000 genomes]
rs11947071	0.84[ASN][1000 genomes]
rs12505156	0.87[ASN][1000 genomes]
rs12508017	0.81[ASN][1000 genomes]
rs12711064	0.82[ASN][1000 genomes]
rs13111697	0.82[ASN][1000 genomes]
rs13114621	0.81[ASN][1000 genomes]
rs13114895	0.81[ASN][1000 genomes]
rs13134901	0.82[ASN][1000 genomes]
rs1319938	0.81[ASN][1000 genomes]
rs1514659	0.81[ASN][1000 genomes]
rs2049362	0.87[ASN][1000 genomes]
rs2140475	0.85[ASN][1000 genomes]
rs2389525	0.81[ASN][1000 genomes]
rs2389526	0.81[ASN][1000 genomes]
rs2389527	0.81[ASN][1000 genomes]
rs2389620	0.83[ASN][1000 genomes]
rs2892791	0.81[ASN][1000 genomes]
rs2892799	0.86[ASN][1000 genomes]
rs4131600	0.82[ASN][1000 genomes]
rs4240316	0.81[ASN][1000 genomes]
rs4240317	0.81[ASN][1000 genomes]
rs4240318	0.81[ASN][1000 genomes]
rs4279285	0.83[ASN][1000 genomes]
rs4280816	0.81[ASN][1000 genomes]
rs4362895	0.86[ASN][1000 genomes]
rs4397073	0.82[ASN][1000 genomes]
rs4452509	0.81[ASN][1000 genomes]
rs4546313	0.92[ASN][1000 genomes]
rs4566725	0.81[ASN][1000 genomes]
rs4569819	0.81[ASN][1000 genomes]
rs4576085	0.81[ASN][1000 genomes]
rs4616829	0.81[ASN][1000 genomes]
rs4833560	0.82[ASN][1000 genomes]
rs4833561	0.82[ASN][1000 genomes]
rs4833563	0.82[ASN][1000 genomes]
rs4833566	0.87[ASN][1000 genomes]
rs4833567	0.92[ASN][1000 genomes]
rs4834657	0.81[ASN][1000 genomes]
rs4834660	0.82[ASN][1000 genomes]
rs4834661	0.82[ASN][1000 genomes]
rs4834664	0.82[ASN][1000 genomes]
rs4834665	0.82[ASN][1000 genomes]
rs4834679	0.83[ASN][1000 genomes]
rs4834681	0.81[ASN][1000 genomes]
rs581739	0.81[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs582448	0.93[ASN][1000 genomes]
rs586073	0.81[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs586224	0.92[ASN][1000 genomes]
rs593966	0.92[ASN][1000 genomes]
rs597881	0.92[ASN][1000 genomes]
rs607961	0.92[ASN][1000 genomes]
rs608228	0.93[ASN][1000 genomes]
rs610222	0.92[ASN][1000 genomes]
rs613083	0.92[ASN][1000 genomes]
rs613443	0.81[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs615837	0.90[ASN][1000 genomes]
rs617140	0.93[ASN][1000 genomes]
rs62328865	0.92[ASN][1000 genomes]
rs62328871	0.93[ASN][1000 genomes]
rs625546	0.91[ASN][1000 genomes]
rs627249	0.93[ASN][1000 genomes]
rs641962	0.92[ASN][1000 genomes]
rs644797	0.87[ASN][1000 genomes]
rs662086	0.92[ASN][1000 genomes]
rs674514	0.92[ASN][1000 genomes]
rs678177	0.92[ASN][1000 genomes]
rs6820061	0.81[ASN][1000 genomes]
rs6823125	0.82[ASN][1000 genomes]
rs6823295	0.82[ASN][1000 genomes]
rs6825105	0.81[ASN][1000 genomes]
rs6828232	0.81[ASN][1000 genomes]
rs6828552	0.82[ASN][1000 genomes]
rs6837896	0.87[ASN][1000 genomes]
rs6842393	0.81[ASN][1000 genomes]
rs6848037	0.81[ASN][1000 genomes]
rs6848598	0.81[ASN][1000 genomes]
rs6851494	0.81[ASN][1000 genomes]
rs6857041	0.82[ASN][1000 genomes]
rs6857232	0.82[ASN][1000 genomes]
rs705838	0.88[ASN][1000 genomes]
rs705841	0.86[ASN][1000 genomes]
rs7435948	0.82[ASN][1000 genomes]
rs7439663	0.81[ASN][1000 genomes]
rs7671232	0.81[ASN][1000 genomes]
rs7671359	0.81[ASN][1000 genomes]
rs7671515	0.81[ASN][1000 genomes]
rs7671562	0.81[ASN][1000 genomes]
rs7679658	0.81[ASN][1000 genomes]
rs7685325	0.82[ASN][1000 genomes]
rs7695706	0.81[ASN][1000 genomes]
rs7699653	0.85[ASN][1000 genomes]
rs788647	0.88[ASN][1000 genomes]
rs788650	0.88[ASN][1000 genomes]
rs788651	0.88[ASN][1000 genomes]
rs788655	0.88[ASN][1000 genomes]
rs788656	0.85[ASN][1000 genomes]
rs788658	0.86[ASN][1000 genomes]
rs788661	0.93[ASN][1000 genomes]
rs788662	0.92[ASN][1000 genomes]
rs788668	0.93[ASN][1000 genomes]
rs788669	0.81[ASN][1000 genomes]
rs9307452	0.82[ASN][1000 genomes]
rs9637622	0.81[ASN][1000 genomes]
rs9637623	0.81[ASN][1000 genomes]
rs9790637	0.81[ASN][1000 genomes]
rs9995675	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519017	chr4:118828807-119771481	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv1009076	chr4:118949490-119269424	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1001236	chr4:118949490-119271243	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	esv34038	chr4:119035124-119455391	Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	nsv1001138	chr4:119095147-119461837	Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv537230	chr4:119095147-119461837	Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv1002771	chr4:119125361-119571237	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
8	nsv1003731	chr4:119138262-119506032	Active TSS Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
9	esv1794655	chr4:119170156-119212103	Active TSS Genic enhancers Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:119177000-119181200	Weak transcription	Stomach Mucosa	stomach
2	chr4:119180600-119185000	Weak transcription	Dnd41	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links