Variant report

Variant	rs73474862
Chromosome Location	chr7:150341555-150341556
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	chr7:150341180..150342757-chr7:150345704..150347785,2	K562	blood:

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:73)

rs_ID	r²[population]
rs11764483	0.82[ASN][1000 genomes]
rs11769703	0.82[ASN][1000 genomes]
rs12154435	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12154436	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12154687	0.89[ASN][1000 genomes]
rs1234356	0.83[ASN][1000 genomes]
rs1234357	0.88[ASN][1000 genomes]
rs1234361	0.82[ASN][1000 genomes]
rs12397707	0.88[ASN][1000 genomes]
rs12532045	0.96[ASN][1000 genomes]
rs12535208	0.89[ASN][1000 genomes]
rs12703091	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1316352	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13220967	0.89[ASN][1000 genomes]
rs13223607	0.82[ASN][1000 genomes]
rs13223653	0.82[ASN][1000 genomes]
rs13225905	0.96[ASN][1000 genomes]
rs13226190	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs13230583	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs13234724	0.86[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs13238412	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs13240099	0.89[ASN][1000 genomes]
rs13240106	0.89[ASN][1000 genomes]
rs1403220	0.96[ASN][1000 genomes]
rs1578916	0.82[ASN][1000 genomes]
rs17542143	0.86[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2204131	0.82[ASN][1000 genomes]
rs34030180	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34079857	0.82[ASN][1000 genomes]
rs34097488	0.82[ASN][1000 genomes]
rs34176120	0.82[ASN][1000 genomes]
rs34396063	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34585329	0.96[ASN][1000 genomes]
rs34940374	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35114152	0.82[ASN][1000 genomes]
rs35233281	0.82[ASN][1000 genomes]
rs35276692	0.82[ASN][1000 genomes]
rs35283918	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35285840	0.96[ASN][1000 genomes]
rs35329030	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35342751	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs35659213	0.82[ASN][1000 genomes]
rs35760614	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs35873531	0.82[ASN][1000 genomes]
rs36020504	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36065681	0.96[ASN][1000 genomes]
rs36200127	0.81[ASN][1000 genomes]
rs3735086	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs3807382	0.82[ASN][1000 genomes]
rs4543461	0.82[ASN][1000 genomes]
rs4573169	0.82[ASN][1000 genomes]
rs55681398	0.83[ASN][1000 genomes]
rs56138121	0.96[ASN][1000 genomes]
rs56279394	0.96[ASN][1000 genomes]
rs56325059	0.86[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs56412316	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57729315	0.82[ASN][1000 genomes]
rs57899656	0.82[ASN][1000 genomes]
rs59468128	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62490361	0.96[ASN][1000 genomes]
rs62490366	0.96[ASN][1000 genomes]
rs62491810	0.80[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs62491812	0.86[AMR][1000 genomes];0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62491814	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62491829	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62502277	0.82[ASN][1000 genomes]
rs62502293	0.82[ASN][1000 genomes]
rs62502294	0.82[ASN][1000 genomes]
rs62503201	0.81[ASN][1000 genomes]
rs6951360	0.82[ASN][1000 genomes]
rs6978778	0.82[ASN][1000 genomes]
rs71539836	0.81[ASN][1000 genomes]
rs954395	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034409	chr7:149844639-150447071	Flanking Active TSS Active TSS Genic enhancers Enhancers ZNF genes & repeats Bivalent Enhancer Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv608990	chr7:149961274-150707488	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	nsv1017368	chr7:150016952-150655773	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
4	nsv539195	chr7:150016952-150655773	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
5	esv2758617	chr7:150251949-150463804	Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
6	esv2759573	chr7:150251949-150463804	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
7	esv3388935	chr7:150301204-150374532	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv1030109	chr7:150312916-150701010	Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
9	nsv967475	chr7:150323577-150610034	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
10	nsv831187	chr7:150325913-150503500	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 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	chr7:150337400-150341800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr7:150338600-150342400	Enhancers	Primary T helper cells PMA-I stimulated	--
3	chr7:150339400-150341800	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr7:150339400-150342400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr7:150340400-150341800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr7:150340400-150341800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr7:150341000-150341800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr7:150341400-150341800	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
9	chr7:150341400-150342200	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr7:150341400-150345000	Enhancers	Primary T helper naive cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links