Variant report

Variant	rs11172775
Chromosome Location	chr12:59257348-59257349
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 62 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10877178	0.82[CHB][hapmap]
rs10877180	0.89[EUR][1000 genomes]
rs10877182	0.82[JPT][hapmap]
rs11172711	0.83[AMR][1000 genomes]
rs11172717	0.88[AMR][1000 genomes]
rs11172727	1.00[CHB][hapmap]
rs11172730	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11172731	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11172737	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11172739	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11172742	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11172759	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11172771	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11172773	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11172774	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11172777	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11172778	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11172779	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11172780	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11172783	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11172784	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11172786	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11172787	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11172790	1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11172791	1.00[CHB][hapmap];0.85[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11172795	0.82[JPT][hapmap]
rs1148531	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11514001	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11514217	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11514219	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11514220	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11514221	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11520079	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11520080	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11520081	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11520082	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11520084	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12366986	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12367092	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12367116	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12367975	0.83[AMR][1000 genomes]
rs12368328	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12369527	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12370599	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12371811	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12372281	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17121454	0.83[AMR][1000 genomes]
rs17121505	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs17121548	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17121569	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17121576	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17121582	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2279718	1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2293659	1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs74099636	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758311	chr12:59022729-59323045	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	esv2759902	chr12:59022729-59323045	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv1043385	chr12:59149582-59758952	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv1067596	chr12:59167152-59764208	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv492251	chr12:59167152-59764208	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
6	nsv1038273	chr12:59232371-59259628	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv3440532	chr12:59244734-59266539	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region miRNA target site	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:59243000-59257600	Weak transcription	NH-A	brain
2	chr12:59243200-59263600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr12:59245200-59257400	Weak transcription	NHDF-Ad	bronchial
4	chr12:59245200-59260000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr12:59250400-59257800	Weak transcription	Gastric	stomach
6	chr12:59251000-59266400	Weak transcription	Esophagus	oesophagus
7	chr12:59251200-59257800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr12:59251200-59261800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr12:59251400-59261400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:59251800-59257600	Weak transcription	HMEC	breast
11	chr12:59251800-59263400	Weak transcription	NHEK	skin
12	chr12:59252200-59259800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr12:59253000-59270200	Weak transcription	Fetal Brain Male	brain
14	chr12:59253400-59265400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr12:59254400-59260000	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr12:59254400-59261600	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr12:59254600-59262000	Weak transcription	Osteobl	bone
18	chr12:59254600-59268600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr12:59254800-59262200	Weak transcription	Stomach Mucosa	stomach
20	chr12:59254800-59266400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr12:59254800-59267000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr12:59255000-59265400	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr12:59255000-59267400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:59255200-59259800	Weak transcription	Fetal Stomach	stomach
25	chr12:59255200-59263400	Weak transcription	Duodenum Mucosa	Duodenum
26	chr12:59255400-59267000	Weak transcription	Pancreas	Pancrea
27	chr12:59255800-59257600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr12:59256000-59261400	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr12:59256200-59257800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr12:59256200-59261800	Weak transcription	NHLF	lung
31	chr12:59256200-59266400	Weak transcription	Left Ventricle	heart
32	chr12:59256400-59261800	Weak transcription	Fetal Muscle Trunk	muscle
33	chr12:59256400-59262200	Weak transcription	Rectal Smooth Muscle	rectum
34	chr12:59256400-59262400	Weak transcription	Muscle Satellite Cultured Cells	--
35	chr12:59256600-59266400	Weak transcription	Stomach Smooth Muscle	stomach
36	chr12:59256800-59263600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr12:59257000-59259600	Weak transcription	Fetal Intestine Small	intestine
38	chr12:59257000-59260000	Weak transcription	Fetal Intestine Large	intestine
39	chr12:59257000-59270800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links