Variant report

Variant	rs73177480
Chromosome Location	chr3:105107665-105107666
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1020110	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10433369	0.90[ASN][1000 genomes]
rs10446292	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10511244	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12186012	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12186024	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12491519	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12495149	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12630634	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12633488	0.85[AFR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12637538	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1347792	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1347793	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1438540	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16844719	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16844723	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16851091	0.82[AFR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16851172	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs16851188	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2007681	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2007688	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2164954	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs5012306	0.88[ASN][1000 genomes]
rs55639861	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56018019	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56052407	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs60073537	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6437591	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6437592	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6437593	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6437594	0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73177460	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73181308	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73183107	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73183124	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73185128	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73185129	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73185131	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73185136	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73185137	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73189029	0.83[ASN][1000 genomes]
rs9637374	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9637375	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9637376	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9637377	0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525071	chr3:105004853-105409321	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv829650	chr3:105070893-105255036	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:105094400-105109000	Weak transcription	Primary hematopoietic stem cells	blood
2	chr3:105104000-105108000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr3:105104200-105108000	Enhancers	HepG2	liver
4	chr3:105105000-105116800	Weak transcription	Aorta	Aorta
5	chr3:105106400-105108600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr3:105106800-105108400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr3:105106800-105108600	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr3:105106800-105108600	Weak transcription	Brain Angular Gyrus	brain
9	chr3:105107000-105108600	Weak transcription	Brain Substantia Nigra	brain
10	chr3:105107000-105110400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr3:105107000-105112800	Weak transcription	NH-A	brain
12	chr3:105107000-105116800	Weak transcription	Osteobl	bone
13	chr3:105107000-105119400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr3:105107400-105108400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr3:105107600-105108000	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr3:105107600-105108000	Enhancers	A549	lung

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