Variant report

Variant	rs12064092
Chromosome Location	chr1:85405389-85405390
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs12022603	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs12032056	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12032915	1.00[CEU][hapmap]
rs12406236	1.00[JPT][hapmap]
rs1325277	0.92[LWK][hapmap];0.93[YRI][hapmap];0.81[AFR][1000 genomes]
rs589332	0.86[YRI][hapmap]
rs666779	0.86[YRI][hapmap]
rs678065	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830448	chr1:85294094-85491110	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv470724	chr1:85334788-85585260	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv462383	chr1:85334788-85594466	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv546700	chr1:85334788-85594466	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv947434	chr1:85334915-85594135	Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85389400-85405600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:85391800-85405800	Weak transcription	Small Intestine	intestine
3	chr1:85395400-85405800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr1:85396400-85410600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr1:85396600-85410800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr1:85399000-85410000	Strong transcription	GM12878-XiMat	blood
7	chr1:85400800-85410800	Weak transcription	Fetal Lung	lung
8	chr1:85402000-85410400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr1:85402000-85419600	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr1:85402200-85410200	Weak transcription	Primary B cells from peripheral blood	blood
11	chr1:85402200-85410400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr1:85403200-85406600	Strong transcription	Rectal Mucosa Donor 31	rectum
13	chr1:85403800-85410800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr1:85404400-85405400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr1:85404400-85405400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr1:85404400-85406600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr1:85404600-85405400	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
18	chr1:85404600-85405800	Strong transcription	Primary T cells fromperipheralblood	blood
19	chr1:85404600-85406600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr1:85404600-85406600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr1:85404600-85406800	Enhancers	NHEK	skin
22	chr1:85404600-85408000	Weak transcription	Spleen	Spleen
23	chr1:85405000-85413200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr1:85405200-85406000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr1:85405200-85406200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr1:85405200-85406200	Weak transcription	Osteobl	bone
27	chr1:85405200-85413000	Weak transcription	Esophagus	oesophagus

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