Variant report

Variant	rs1717542
Chromosome Location	chr10:59011037-59011038
allele	A/C
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:79)

rs_ID	r²[population]
rs10509071	0.88[ASN][1000 genomes]
rs10740697	0.95[ASN][1000 genomes]
rs10763458	0.90[ASN][1000 genomes]
rs10763459	0.93[ASN][1000 genomes]
rs10763460	0.93[ASN][1000 genomes]
rs10763461	0.93[ASN][1000 genomes]
rs10825997	0.90[ASN][1000 genomes]
rs10825998	0.90[ASN][1000 genomes]
rs10825999	0.90[ASN][1000 genomes]
rs10826000	0.90[ASN][1000 genomes]
rs10826001	0.89[ASN][1000 genomes]
rs10826002	0.93[ASN][1000 genomes]
rs11005690	0.90[ASN][1000 genomes]
rs11005693	0.90[ASN][1000 genomes]
rs11005694	0.90[ASN][1000 genomes]
rs11005697	0.93[ASN][1000 genomes]
rs11005698	0.93[ASN][1000 genomes]
rs11005705	0.93[ASN][1000 genomes]
rs11005707	0.93[ASN][1000 genomes]
rs11813074	0.90[ASN][1000 genomes]
rs11817602	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12241230	0.90[ASN][1000 genomes]
rs12248556	0.90[ASN][1000 genomes]
rs12253845	0.90[ASN][1000 genomes]
rs12256265	0.93[ASN][1000 genomes]
rs12262622	0.90[ASN][1000 genomes]
rs12263669	0.90[ASN][1000 genomes]
rs1275273	0.95[ASN][1000 genomes]
rs1394113	0.93[ASN][1000 genomes]
rs1503918	0.93[ASN][1000 genomes]
rs1587779	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1614490	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1615297	0.95[ASN][1000 genomes]
rs1631310	0.95[ASN][1000 genomes]
rs1679473	0.95[ASN][1000 genomes]
rs1679474	0.95[ASN][1000 genomes]
rs1679475	0.95[ASN][1000 genomes]
rs1717543	0.98[ASN][1000 genomes]
rs1717545	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1717546	0.95[ASN][1000 genomes]
rs1949643	0.93[ASN][1000 genomes]
rs1949644	0.93[ASN][1000 genomes]
rs2055552	0.90[ASN][1000 genomes]
rs2055553	0.90[ASN][1000 genomes]
rs2055554	0.90[ASN][1000 genomes]
rs2134715	0.93[ASN][1000 genomes]
rs2393226	0.88[ASN][1000 genomes]
rs2893721	0.88[ASN][1000 genomes]
rs2938357	0.95[ASN][1000 genomes]
rs35160997	0.84[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4142773	0.90[ASN][1000 genomes]
rs4935159	0.90[ASN][1000 genomes]
rs4935160	0.90[ASN][1000 genomes]
rs4935690	0.93[ASN][1000 genomes]
rs4935691	0.80[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs56401017	0.95[ASN][1000 genomes]
rs57964207	0.90[ASN][1000 genomes]
rs6481260	0.90[ASN][1000 genomes]
rs6481261	0.90[ASN][1000 genomes]
rs6481262	0.93[ASN][1000 genomes]
rs7068788	0.90[ASN][1000 genomes]
rs7071075	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7073031	0.90[ASN][1000 genomes]
rs7073183	0.90[ASN][1000 genomes]
rs7076175	0.95[ASN][1000 genomes]
rs7077270	0.90[ASN][1000 genomes]
rs7077365	0.93[ASN][1000 genomes]
rs7079010	0.90[ASN][1000 genomes]
rs7079023	0.84[ASN][1000 genomes]
rs7082837	0.90[ASN][1000 genomes]
rs7083404	0.90[ASN][1000 genomes]
rs7084661	0.90[ASN][1000 genomes]
rs7085848	0.90[ASN][1000 genomes]
rs7090028	0.90[ASN][1000 genomes]
rs7095249	0.90[ASN][1000 genomes]
rs7095592	0.93[ASN][1000 genomes]
rs7098302	0.90[ASN][1000 genomes]
rs7905435	0.90[ASN][1000 genomes]
rs7905550	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2756345	chr10:58846594-59027194	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv895543	chr10:58938552-59210800	Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv895544	chr10:58938552-59282980	Weak transcription Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
4	nsv895545	chr10:58938552-59313872	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases
5	nsv916857	chr10:58960110-59272160	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:59010800-59011400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr10:59011000-59013000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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