Variant report

Variant	rs1385306
Chromosome Location	chr3:136739406-136739407
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:136734281..136736785-chr3:136737502..136739437,2	K562	blood:

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs108858	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11711599	0.82[ASN][1000 genomes]
rs13095034	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1470142	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1654900	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1654901	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1682361	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1682362	0.95[AMR][1000 genomes];0.99[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	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	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs171519	0.82[ASN][1000 genomes]
rs181732	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs183120	0.82[ASN][1000 genomes]
rs2086880	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2117008	0.85[AFR][1000 genomes];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	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs361233	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs361234	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs361235	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[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];0.90[EUR][1000 genomes]
rs4678281	0.88[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	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6763000	0.82[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	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs754694	0.90[EUR][1000 genomes]
rs7640951	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7646307	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs835627	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];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs835652	0.87[AMR][1000 genomes];0.95[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];0.92[EUR][1000 genomes]
rs900949	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs900950	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9681468	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9817061	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9827066	0.90[EUR][1000 genomes]
rs9845076	0.89[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	0.87[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:15 , 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	chr3:136733600-136742400	Weak transcription	HSMM	muscle
4	chr3:136733800-136742200	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr3:136735400-136742200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr3:136738400-136741400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr3:136738400-136748600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr3:136738600-136740400	Enhancers	Liver	Liver
9	chr3:136739000-136741200	Strong transcription	NHEK	skin
10	chr3:136739200-136739600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr3:136739200-136739600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:136739200-136739600	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr3:136739200-136739800	Enhancers	HSMMtube	muscle
14	chr3:136739400-136741600	Weak transcription	HepG2	liver
15	chr3:136739400-136742200	Weak transcription	Fetal Muscle Leg	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links