Variant report

Variant	rs10505091
Chromosome Location	chr8:106954208-106954209
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:106952696..106955159-chr8:106958008..106960876,3	K562	blood:
2	chr8:106953058..106955739-chr8:107063560..107065111,2	K562	blood:

Extended variants
information (count: 115 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:111)

rs_ID	r²[population]
rs10086055	0.91[ASN][1000 genomes]
rs10092927	0.99[ASN][1000 genomes]
rs1032545	0.93[ASN][1000 genomes]
rs10808408	0.93[ASN][1000 genomes]
rs10955407	0.92[ASN][1000 genomes]
rs10955408	0.91[ASN][1000 genomes]
rs10955409	0.92[ASN][1000 genomes]
rs11781234	0.93[ASN][1000 genomes]
rs11782609	0.99[ASN][1000 genomes]
rs11786829	0.92[ASN][1000 genomes]
rs12542361	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12542647	0.90[CHB][hapmap]
rs12546875	0.93[ASN][1000 genomes]
rs12674846	0.94[ASN][1000 genomes]
rs12675478	0.95[ASN][1000 genomes]
rs12676365	0.82[CEU][hapmap];0.86[CHB][hapmap]
rs12677927	0.91[ASN][1000 genomes]
rs12680670	0.94[ASN][1000 genomes]
rs12681183	0.94[ASN][1000 genomes]
rs13274603	0.84[CEU][hapmap]
rs13439705	0.98[ASN][1000 genomes]
rs1353449	0.85[CHB][hapmap]
rs1353450	0.92[ASN][1000 genomes]
rs1429681	0.91[ASN][1000 genomes]
rs1496180	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1496181	0.91[ASN][1000 genomes]
rs1496182	0.92[ASN][1000 genomes]
rs1496183	0.91[ASN][1000 genomes]
rs1603357	0.94[ASN][1000 genomes]
rs1603363	0.92[ASN][1000 genomes]
rs16873932	0.85[EUR][1000 genomes]
rs16873989	0.99[ASN][1000 genomes]
rs1817939	0.91[ASN][1000 genomes]
rs1835267	0.92[ASN][1000 genomes]
rs1835268	0.88[ASN][1000 genomes]
rs2029878	0.91[ASN][1000 genomes]
rs2029879	0.91[ASN][1000 genomes]
rs2029880	0.91[ASN][1000 genomes]
rs2029881	0.96[ASN][1000 genomes]
rs2029882	0.92[ASN][1000 genomes]
rs2059943	0.89[ASN][1000 genomes]
rs2115703	0.92[ASN][1000 genomes]
rs2132471	0.96[ASN][1000 genomes]
rs2163124	0.91[ASN][1000 genomes]
rs2172997	0.93[ASN][1000 genomes]
rs2217391	0.91[ASN][1000 genomes]
rs2345068	0.93[ASN][1000 genomes]
rs2345070	0.86[ASN][1000 genomes]
rs34177605	0.91[ASN][1000 genomes]
rs34872724	0.91[ASN][1000 genomes]
rs4416800	0.96[ASN][1000 genomes]
rs4734126	0.99[ASN][1000 genomes]
rs4734128	0.92[ASN][1000 genomes]
rs4734892	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs4734893	0.96[ASN][1000 genomes]
rs4734894	0.96[ASN][1000 genomes]
rs4734895	0.96[ASN][1000 genomes]
rs55639043	0.91[ASN][1000 genomes]
rs55729609	0.92[ASN][1000 genomes]
rs55762012	0.92[ASN][1000 genomes]
rs55811614	0.99[ASN][1000 genomes]
rs56352125	0.92[ASN][1000 genomes]
rs56402027	0.92[ASN][1000 genomes]
rs57607757	0.99[ASN][1000 genomes]
rs57715289	0.99[ASN][1000 genomes]
rs59123253	0.94[ASN][1000 genomes]
rs59858392	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs60482457	0.98[ASN][1000 genomes]
rs62525696	0.99[ASN][1000 genomes]
rs62525736	0.96[ASN][1000 genomes]
rs62527360	0.91[ASN][1000 genomes]
rs62527363	0.92[ASN][1000 genomes]
rs62527373	0.92[ASN][1000 genomes]
rs62527374	0.92[ASN][1000 genomes]
rs62527375	0.87[ASN][1000 genomes]
rs62527376	0.92[ASN][1000 genomes]
rs62527400	0.92[ASN][1000 genomes]
rs62527405	0.91[ASN][1000 genomes]
rs6415444	0.88[ASN][1000 genomes]
rs6469023	0.96[ASN][1000 genomes]
rs6469026	0.93[ASN][1000 genomes]
rs6469027	0.91[ASN][1000 genomes]
rs6469028	0.94[ASN][1000 genomes]
rs6469030	0.91[ASN][1000 genomes]
rs6469031	0.88[ASN][1000 genomes]
rs6469032	0.91[ASN][1000 genomes]
rs6469038	0.91[CEU][hapmap]
rs6984393	0.86[ASN][1000 genomes]
rs6987512	0.96[ASN][1000 genomes]
rs6997487	0.98[ASN][1000 genomes]
rs6999580	0.91[ASN][1000 genomes]
rs7003520	0.91[ASN][1000 genomes]
rs7008840	0.92[ASN][1000 genomes]
rs7012379	0.80[ASN][1000 genomes]
rs7013082	0.85[CHB][hapmap]
rs72676052	0.92[ASN][1000 genomes]
rs727419	0.91[CEU][hapmap]
rs7460291	0.91[ASN][1000 genomes]
rs7812766	0.91[ASN][1000 genomes]
rs7814776	0.81[CHB][hapmap]
rs7815337	0.88[ASN][1000 genomes]
rs7819043	0.96[ASN][1000 genomes]
rs7819501	0.93[ASN][1000 genomes]
rs7829054	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7830426	0.91[ASN][1000 genomes]
rs7836196	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7839195	0.91[ASN][1000 genomes]
rs7839239	0.89[ASN][1000 genomes]
rs7843166	0.91[ASN][1000 genomes]
rs7846149	0.91[ASN][1000 genomes]
rs7846262	0.92[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	nsv1021369	chr8:106493317-107243322	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv611840	chr8:106913294-107265915	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1019518	chr8:106923469-106959075	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv515580	chr8:106925995-106956427	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:106952400-106957200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr8:106952800-106957400	Weak transcription	Osteobl	bone
3	chr8:106954000-106954400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links