Variant report

Variant	rs12244390
Chromosome Location	chr10:118261421-118261422
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 84 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:81)

rs_ID	r²[population]
rs10458761	0.87[ASN][1000 genomes]
rs10458763	0.91[ASN][1000 genomes]
rs10510022	0.84[ASN][1000 genomes]
rs10510023	0.85[ASN][1000 genomes]
rs10749219	0.92[ASN][1000 genomes]
rs10787679	0.91[ASN][1000 genomes]
rs10787680	0.92[ASN][1000 genomes]
rs10787685	0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs10787706	0.85[ASN][1000 genomes]
rs10787707	0.84[ASN][1000 genomes]
rs10787708	0.85[ASN][1000 genomes]
rs10885941	0.89[ASN][1000 genomes]
rs10885964	0.91[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs10885965	0.87[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs10885981	0.85[ASN][1000 genomes]
rs11197690	0.85[ASN][1000 genomes]
rs11197694	0.92[ASN][1000 genomes]
rs11197707	0.89[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs11197711	0.95[ASN][1000 genomes]
rs11197712	0.94[ASN][1000 genomes]
rs11197728	0.84[ASN][1000 genomes]
rs11197729	0.85[ASN][1000 genomes]
rs11525278	0.93[ASN][1000 genomes]
rs11525290	0.93[ASN][1000 genomes]
rs11812945	0.92[ASN][1000 genomes]
rs11813385	0.92[ASN][1000 genomes]
rs11815357	0.88[ASN][1000 genomes]
rs11817431	0.85[ASN][1000 genomes]
rs11817441	0.83[ASN][1000 genomes]
rs11817470	0.85[ASN][1000 genomes]
rs12217917	0.84[ASN][1000 genomes]
rs12220096	0.84[ASN][1000 genomes]
rs12221345	0.84[ASN][1000 genomes]
rs12244215	0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs12264355	0.89[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs12761687	0.87[ASN][1000 genomes]
rs12767361	0.91[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs17094828	0.92[ASN][1000 genomes]
rs17094927	0.83[ASN][1000 genomes]
rs2420293	0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2420294	0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs2420295	0.85[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2420296	0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2420297	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2420298	0.93[ASN][1000 genomes]
rs2420299	0.86[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs2901107	0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs4357611	0.85[ASN][1000 genomes]
rs4454634	0.80[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs4491137	0.85[ASN][1000 genomes]
rs4751597	0.91[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs4751598	0.91[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs4751599	0.90[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs4751600	0.84[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs4751601	0.90[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs4751975	0.92[ASN][1000 genomes]
rs4751982	0.91[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs55989001	0.88[ASN][1000 genomes]
rs56755358	0.89[ASN][1000 genomes]
rs58380571	0.91[ASN][1000 genomes]
rs58623886	0.91[ASN][1000 genomes]
rs58834459	0.92[ASN][1000 genomes]
rs59690687	0.85[ASN][1000 genomes]
rs59775092	0.91[ASN][1000 genomes]
rs6585410	0.83[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs66492245	0.91[ASN][1000 genomes]
rs68098419	0.83[ASN][1000 genomes]
rs7070270	0.85[ASN][1000 genomes]
rs7081675	0.86[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs7094130	0.87[ASN][1000 genomes]
rs7097727	0.89[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs7097841	0.93[ASN][1000 genomes]
rs7098296	0.86[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs72823429	0.91[ASN][1000 genomes]
rs7894218	0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs7894682	0.95[ASN][1000 genomes]
rs7910824	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7914091	0.85[ASN][1000 genomes]
rs7922996	0.92[ASN][1000 genomes]
rs7923127	0.92[ASN][1000 genomes]
rs9943371	0.94[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	nsv832001	chr10:118138370-118315059	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv3415357	chr10:118254861-118383651	Weak transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv2754784	chr10:118255010-118284010	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:118258800-118262400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links