Variant report

Variant	rs1345026
Chromosome Location	chr9:21745756-21745757
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 137 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:133)

rs_ID	r²[population]
rs10118262	0.84[ASN][1000 genomes]
rs10119658	0.84[ASN][1000 genomes]
rs10738596	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10738597	0.90[ASN][1000 genomes]
rs10738599	0.82[ASN][1000 genomes]
rs10757236	0.81[ASN][1000 genomes]
rs10757238	0.88[ASN][1000 genomes]
rs10757239	0.88[ASN][1000 genomes]
rs10757240	0.88[ASN][1000 genomes]
rs10757241	0.88[ASN][1000 genomes]
rs10757242	0.89[ASN][1000 genomes]
rs10757245	0.90[ASN][1000 genomes]
rs10757246	0.90[ASN][1000 genomes]
rs10757247	0.90[ASN][1000 genomes]
rs10757250	0.86[ASN][1000 genomes]
rs10757251	0.85[ASN][1000 genomes]
rs10757252	0.86[ASN][1000 genomes]
rs10757253	0.82[ASN][1000 genomes]
rs10757254	0.82[ASN][1000 genomes]
rs10757255	0.82[ASN][1000 genomes]
rs10811592	0.81[ASN][1000 genomes]
rs10811595	0.81[ASN][1000 genomes]
rs10811600	0.88[ASN][1000 genomes]
rs10811601	0.88[ASN][1000 genomes]
rs10811602	0.88[ASN][1000 genomes]
rs10811604	0.89[ASN][1000 genomes]
rs10811605	0.89[ASN][1000 genomes]
rs10811613	0.82[ASN][1000 genomes]
rs10965122	0.82[ASN][1000 genomes]
rs10965127	0.82[ASN][1000 genomes]
rs1335502	0.88[ASN][1000 genomes]
rs1335505	0.95[CHB][hapmap];0.87[ASN][1000 genomes]
rs1335506	0.87[ASN][1000 genomes]
rs1335507	0.87[ASN][1000 genomes]
rs1335508	0.87[ASN][1000 genomes]
rs1335512	0.82[ASN][1000 genomes]
rs1345027	0.86[ASN][1000 genomes]
rs1372057	0.95[CHB][hapmap];0.90[ASN][1000 genomes]
rs1372058	0.95[CHB][hapmap];0.90[ASN][1000 genomes]
rs1372059	0.95[CHB][hapmap];0.90[ASN][1000 genomes]
rs1414228	0.82[ASN][1000 genomes]
rs1414229	0.82[ASN][1000 genomes]
rs1414236	0.87[ASN][1000 genomes]
rs1414237	0.88[ASN][1000 genomes]
rs1414238	0.88[ASN][1000 genomes]
rs1414242	0.94[CHB][hapmap];0.87[ASN][1000 genomes]
rs1414244	0.95[CHB][hapmap];0.87[ASN][1000 genomes]
rs1414245	0.87[ASN][1000 genomes]
rs1414246	0.87[ASN][1000 genomes]
rs1414247	0.87[ASN][1000 genomes]
rs1414248	0.87[ASN][1000 genomes]
rs1414249	0.87[ASN][1000 genomes]
rs1414250	0.84[ASN][1000 genomes]
rs1414251	0.84[ASN][1000 genomes]
rs1414252	0.84[ASN][1000 genomes]
rs1414256	0.84[ASN][1000 genomes]
rs1414257	0.84[ASN][1000 genomes]
rs1440993	0.82[ASN][1000 genomes]
rs1542075	0.84[CHB][hapmap]
rs1542076	0.84[CHB][hapmap]
rs17833407	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[ASN][1000 genomes]
rs1932237	0.84[ASN][1000 genomes]
rs1965153	0.87[ASN][1000 genomes]
rs2027162	0.89[ASN][1000 genomes]
rs2027163	0.89[ASN][1000 genomes]
rs2043991	0.84[ASN][1000 genomes]
rs2119466	0.90[ASN][1000 genomes]
rs2119467	0.90[ASN][1000 genomes]
rs2152272	0.81[ASN][1000 genomes]
rs2152273	0.82[ASN][1000 genomes]
rs2165408	0.83[CHB][hapmap]
rs2165411	0.84[ASN][1000 genomes]
rs2184551	0.82[ASN][1000 genomes]
rs2218220	0.84[ASN][1000 genomes]
rs2891159	0.94[CHB][hapmap];0.90[ASN][1000 genomes]
rs2891160	0.88[ASN][1000 genomes]
rs3849929	0.82[ASN][1000 genomes]
rs3928894	0.83[CHB][hapmap]
rs4300088	0.84[ASN][1000 genomes]
rs4350062	0.88[ASN][1000 genomes]
rs4352937	0.95[CHB][hapmap];0.88[ASN][1000 genomes]
rs4364717	0.83[CHB][hapmap]
rs4384075	0.87[ASN][1000 genomes]
rs4548267	0.94[CHB][hapmap];0.87[ASN][1000 genomes]
rs4636294	0.89[CHB][hapmap];0.90[ASN][1000 genomes]
rs62558566	0.91[ASN][1000 genomes]
rs62559378	0.98[ASN][1000 genomes]
rs6475554	0.81[ASN][1000 genomes]
rs6475555	0.81[ASN][1000 genomes]
rs6475564	0.84[ASN][1000 genomes]
rs6475566	0.88[ASN][1000 genomes]
rs6475568	0.88[ASN][1000 genomes]
rs6475569	0.88[ASN][1000 genomes]
rs6475571	0.86[ASN][1000 genomes]
rs6475572	0.86[ASN][1000 genomes]
rs6475574	0.87[ASN][1000 genomes]
rs6475576	0.83[ASN][1000 genomes]
rs6475578	0.82[ASN][1000 genomes]
rs6475579	0.82[ASN][1000 genomes]
rs6475585	0.88[CHB][hapmap]
rs7021012	0.84[ASN][1000 genomes]
rs7021538	0.88[ASN][1000 genomes]
rs7023299	0.84[ASN][1000 genomes]
rs7023474	0.81[CEU][hapmap];0.83[CHB][hapmap]
rs7024027	0.82[ASN][1000 genomes]
rs7028913	0.81[ASN][1000 genomes]
rs7029040	0.81[ASN][1000 genomes]
rs7029166	0.81[ASN][1000 genomes]
rs7029274	0.81[ASN][1000 genomes]
rs7037577	0.81[ASN][1000 genomes]
rs7043827	0.84[ASN][1000 genomes]
rs7045768	0.82[ASN][1000 genomes]
rs7850446	0.83[ASN][1000 genomes]
rs7852710	0.84[ASN][1000 genomes]
rs7852900	0.90[ASN][1000 genomes]
rs7853131	0.90[ASN][1000 genomes]
rs7854018	0.88[ASN][1000 genomes]
rs7854222	0.87[ASN][1000 genomes]
rs7855242	0.84[ASN][1000 genomes]
rs7856941	0.81[ASN][1000 genomes]
rs7858991	0.88[ASN][1000 genomes]
rs7860576	0.81[ASN][1000 genomes]
rs7866540	0.84[ASN][1000 genomes]
rs7866787	0.82[ASN][1000 genomes]
rs7866885	0.81[ASN][1000 genomes]
rs7871345	0.84[ASN][1000 genomes]
rs7874319	0.88[ASN][1000 genomes]
rs869330	0.83[CHB][hapmap]
rs871024	0.83[CHB][hapmap]
rs9298823	0.95[CHB][hapmap];0.87[ASN][1000 genomes]
rs9298824	0.87[ASN][1000 genomes]
rs9298825	0.86[ASN][1000 genomes]
rs9886831	0.82[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	nsv1029634	chr9:21542970-21765286	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv892743	chr9:21675545-21772064	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv892744	chr9:21694039-21746419	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv529609	chr9:21708371-22537069	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 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	chr9:21743200-21750000	Weak transcription	NH-A	brain
2	chr9:21743400-21750000	Weak transcription	Osteobl	bone
3	chr9:21744200-21747400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr9:21744200-21747400	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr9:21744200-21752200	Enhancers	HMEC	breast
6	chr9:21745000-21748800	Enhancers	NHEK	skin
7	chr9:21745400-21745800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr9:21745400-21746600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr9:21745400-21746800	Weak transcription	Hela-S3	cervix
10	chr9:21745400-21747200	Weak transcription	NHDF-Ad	bronchial
11	chr9:21745600-21746600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr9:21745600-21746600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr9:21745600-21746600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr9:21745600-21746600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr9:21745600-21746600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr9:21745600-21747200	Weak transcription	Muscle Satellite Cultured Cells	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links