Variant report

Variant	rs712307
Chromosome Location	chr14:35396035-35396036
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:35347496..35349428-chr14:35395723..35397299,2	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs1028449	0.86[JPT][hapmap]
rs12050171	0.80[ASN][1000 genomes]
rs12878219	0.91[JPT][hapmap]
rs12887885	0.91[JPT][hapmap]
rs12891343	0.91[JPT][hapmap]
rs12895051	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs17102967	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs17102970	0.83[CHB][hapmap];0.85[JPT][hapmap]
rs1712349	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1738801	0.99[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1967723	0.85[CHB][hapmap];0.85[JPT][hapmap]
rs2143950	0.82[JPT][hapmap]
rs2273158	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs2383688	0.80[ASN][1000 genomes]
rs2383689	0.83[CHB][hapmap];0.86[JPT][hapmap];0.80[ASN][1000 genomes]
rs3809449	0.86[JPT][hapmap]
rs4594164	0.86[JPT][hapmap]
rs712302	0.98[ASN][1000 genomes]
rs712303	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs712304	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs712306	1.00[ASN][1000 genomes]
rs712308	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs712309	1.00[ASN][1000 genomes]
rs712311	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs712312	0.97[ASN][1000 genomes]
rs7144423	0.86[JPT][hapmap]
rs7144617	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs7145474	0.86[JPT][hapmap]
rs7153068	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs7153550	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs7156322	0.86[JPT][hapmap]
rs799453	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs799462	0.98[ASN][1000 genomes]
rs799463	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs799664	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8014377	0.86[JPT][hapmap]
rs8017225	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs8018114	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs8019179	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs932473	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs941653	0.86[JPT][hapmap]

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	nsv1041857	chr14:35084889-35417180	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
2	nsv1052162	chr14:35245349-35451187	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
3	nsv1053722	chr14:35257458-35465784	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
4	nsv1045939	chr14:35311074-35494703	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
5	nsv456203	chr14:35311272-35512335	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
6	nsv564200	chr14:35311272-35512335	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
7	nsv901602	chr14:35367889-35571651	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
8	nsv901603	chr14:35371697-35435651	Strong transcription Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv949617	chr14:35379923-35825436	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
10	nsv901604	chr14:35381137-35485748	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35381000-35398600	Weak transcription	Primary T cells from cord blood	blood
2	chr14:35381400-35412200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr14:35384600-35398200	Weak transcription	Primary T cells fromperipheralblood	blood
4	chr14:35384800-35398600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr14:35387400-35397000	Weak transcription	Fetal Intestine Small	intestine
6	chr14:35389600-35411400	Weak transcription	Aorta	Aorta
7	chr14:35390000-35412600	Weak transcription	Ovary	ovary
8	chr14:35390200-35400600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr14:35393000-35404400	Weak transcription	Left Ventricle	heart
10	chr14:35394600-35424000	Weak transcription	Fetal Lung	lung
11	chr14:35394800-35398200	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr14:35395000-35396600	Enhancers	HUVEC	blood vessel
13	chr14:35395200-35398200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
14	chr14:35395200-35398200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr14:35395400-35396400	Enhancers	Osteobl	bone
16	chr14:35395600-35396200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr14:35395600-35396400	Enhancers	Muscle Satellite Cultured Cells	--
18	chr14:35395600-35396400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr14:35395600-35399400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr14:35396000-35400400	Weak transcription	A549	lung

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