Variant report

Variant	rs496436
Chromosome Location	chr3:43079390-43079391
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs13061038	0.86[ASN][1000 genomes]
rs13095711	0.99[ASN][1000 genomes]
rs2280565	0.83[CHB][hapmap];0.88[JPT][hapmap];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2936817	0.81[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs34970115	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35339908	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs473467	0.89[CHB][hapmap];0.88[JPT][hapmap];0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs477594	0.86[CHB][hapmap];0.86[JPT][hapmap];0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs504973	0.89[CHB][hapmap];0.88[JPT][hapmap];0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs536119	0.88[CHB][hapmap];0.94[JPT][hapmap];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs536572	0.82[CHB][hapmap]
rs56009835	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs590899	0.88[CHB][hapmap]
rs606336	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62247065	0.80[ASN][1000 genomes]
rs643663	0.95[ASN][1000 genomes]
rs648273	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs658958	1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs660324	0.82[CHB][hapmap]
rs660446	0.89[CHB][hapmap];0.88[JPT][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6806706	0.88[JPT][hapmap];0.80[ASN][1000 genomes]
rs693290	0.83[CHB][hapmap]
rs697327	0.82[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs834188	0.81[CHB][hapmap]
rs870238	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs9311333	0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs9882262	0.94[JPT][hapmap];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460522	chr3:42967597-43175207	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv590149	chr3:42967597-43175207	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv432417	chr3:43045796-43098296	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv979824	chr3:43079103-43080204	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:43059600-43084600	Weak transcription	Pancreas	Pancrea
2	chr3:43061000-43080200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr3:43063600-43084800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr3:43065400-43084400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr3:43067600-43084000	Weak transcription	Aorta	Aorta
6	chr3:43070600-43084800	Weak transcription	Esophagus	oesophagus
7	chr3:43073400-43084600	Weak transcription	Brain Angular Gyrus	brain
8	chr3:43073400-43084600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr3:43073600-43084400	Weak transcription	Adipose Nuclei	Adipose
10	chr3:43074600-43084200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr3:43074800-43081200	Weak transcription	Fetal Intestine Small	intestine
12	chr3:43075200-43084200	Weak transcription	Ovary	ovary
13	chr3:43077200-43084400	Weak transcription	Stomach Smooth Muscle	stomach
14	chr3:43077600-43084600	Weak transcription	Fetal Muscle Trunk	muscle
15	chr3:43077800-43080000	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr3:43078400-43084200	Weak transcription	Placenta	Placenta
17	chr3:43078800-43084200	Weak transcription	Liver	Liver
18	chr3:43078800-43084400	Weak transcription	Fetal Stomach	stomach
19	chr3:43079000-43079400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr3:43079000-43080400	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr3:43079000-43085400	Weak transcription	Fetal Muscle Leg	muscle
22	chr3:43079200-43079600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr3:43079200-43080600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr3:43079200-43080600	Enhancers	Primary T helper cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links