Variant report

Variant	rs1682362
Chromosome Location	chr3:136735607-136735608
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:136467223..136474337-chr3:136727110..136735930,17	K562	blood:
2	chr3:136734281..136736785-chr3:136737502..136739437,2	K562	blood:
3	chr3:136467223..136474007-chr3:136729764..136735930,11	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL20RB-2	chr3:136734713-136735851	NONHSAT092298

Variant related genes	Relation type
ENSG00000118007	Chromatin interaction
ENSG00000261758	Chromatin interaction

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs108858	0.86[CHB][hapmap];0.92[JPT][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11711599	0.82[ASN][1000 genomes]
rs13095034	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1385306	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1470142	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1654900	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1654901	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1682361	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1682363	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1682364	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1682365	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1682366	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16844241	0.82[CHB][hapmap]
rs171519	0.82[ASN][1000 genomes]
rs181732	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs183120	0.82[ASN][1000 genomes]
rs2086880	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2117008	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2344092	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34564994	0.88[EUR][1000 genomes]
rs361227	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs361228	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs361229	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs361231	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs361232	0.86[CHB][hapmap];0.92[JPT][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs361233	0.86[CHB][hapmap];0.92[JPT][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs361234	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs361235	0.86[CHB][hapmap];0.92[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs361238	0.82[ASN][1000 genomes]
rs361240	0.82[ASN][1000 genomes]
rs361249	0.82[ASN][1000 genomes]
rs361253	0.82[ASN][1000 genomes]
rs4678278	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4678281	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55781515	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6439677	0.90[EUR][1000 genomes]
rs6439678	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6763000	0.86[AMR][1000 genomes]
rs6763556	0.83[AMR][1000 genomes]
rs6766766	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6766858	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6802479	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs71620537	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs754694	0.89[EUR][1000 genomes]
rs7640951	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7646307	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs835627	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs835628	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs835629	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs835630	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs835631	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs835651	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs835652	0.86[CHB][hapmap];0.91[JPT][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs900947	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs900948	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs900949	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs900950	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9681468	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9817061	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9827066	0.89[EUR][1000 genomes]
rs9845076	0.86[CHB][hapmap];0.92[JPT][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9850024	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9854795	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9874615	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9875855	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs999038	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877534	chr3:136676303-136765859	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv524856	chr3:136693459-137190765	Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1012111	chr3:136695367-137343430	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:136733200-136742200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr3:136733400-136742400	Weak transcription	Esophagus	oesophagus
3	chr3:136733600-136738400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr3:136733600-136739200	Weak transcription	HSMMtube	muscle
5	chr3:136733600-136742400	Weak transcription	HSMM	muscle
6	chr3:136733800-136736000	Enhancers	Liver	Liver
7	chr3:136733800-136738400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr3:136733800-136739000	Weak transcription	NHEK	skin
9	chr3:136733800-136739200	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr3:136733800-136742200	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr3:136734200-136739000	Weak transcription	HepG2	liver
12	chr3:136734400-136739200	Weak transcription	Fetal Muscle Leg	muscle
13	chr3:136735200-136735800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr3:136735400-136742200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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