Variant report

Variant	rs10462082
Chromosome Location	chr5:44800917-44800918
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:44800337..44802609-chr5:44815368..44818346,2	K562	blood:
2	chr5:44799408..44802083-chr5:44803871..44806335,2	K562	blood:

Extended variants
information (count: 159 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:148)

rs_ID	r²[population]
rs10038562	0.95[ASN][1000 genomes]
rs10040082	0.92[ASN][1000 genomes]
rs10040488	0.88[ASN][1000 genomes]
rs10041518	0.88[ASN][1000 genomes]
rs10044096	0.84[ASN][1000 genomes]
rs10045264	0.86[ASN][1000 genomes]
rs10057521	0.90[ASN][1000 genomes]
rs10059086	0.88[ASN][1000 genomes]
rs10060878	0.87[ASN][1000 genomes]
rs10063172	0.81[ASN][1000 genomes]
rs10064434	0.91[ASN][1000 genomes]
rs10064437	0.92[ASN][1000 genomes]
rs10065638	0.92[ASN][1000 genomes]
rs10069220	0.88[ASN][1000 genomes]
rs10070037	0.88[ASN][1000 genomes]
rs10072025	0.95[ASN][1000 genomes]
rs10072259	0.83[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs10462080	0.97[ASN][1000 genomes]
rs10462081	0.89[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs10462083	0.97[ASN][1000 genomes]
rs10473376	0.81[ASN][1000 genomes]
rs10473377	0.81[ASN][1000 genomes]
rs1048758	0.90[ASN][1000 genomes]
rs10512865	0.91[ASN][1000 genomes]
rs1061310	0.93[ASN][1000 genomes]
rs11741772	0.89[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs11746506	0.97[ASN][1000 genomes]
rs11746980	0.92[ASN][1000 genomes]
rs11747159	0.87[ASN][1000 genomes]
rs11750119	0.94[ASN][1000 genomes]
rs11948387	0.87[ASN][1000 genomes]
rs11948636	0.88[ASN][1000 genomes]
rs11949847	0.90[ASN][1000 genomes]
rs11951760	0.88[ASN][1000 genomes]
rs11957920	0.85[ASN][1000 genomes]
rs11958451	0.88[ASN][1000 genomes]
rs12109710	0.81[ASN][1000 genomes]
rs12188871	0.89[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs12513749	0.92[ASN][1000 genomes]
rs12517690	0.80[ASN][1000 genomes]
rs12518851	0.95[ASN][1000 genomes]
rs12651949	0.97[ASN][1000 genomes]
rs12652026	0.97[ASN][1000 genomes]
rs12656984	0.91[ASN][1000 genomes]
rs13154781	0.95[ASN][1000 genomes]
rs13155698	0.95[ASN][1000 genomes]
rs13157608	0.87[ASN][1000 genomes]
rs13159598	0.93[ASN][1000 genomes]
rs13160259	0.88[ASN][1000 genomes]
rs13168400	0.88[ASN][1000 genomes]
rs13174122	0.93[ASN][1000 genomes]
rs13177711	0.92[ASN][1000 genomes]
rs13183209	0.97[ASN][1000 genomes]
rs13185174	0.95[ASN][1000 genomes]
rs13187933	0.88[ASN][1000 genomes]
rs13189120	0.96[ASN][1000 genomes]
rs1371023	0.91[ASN][1000 genomes]
rs1371024	0.94[ASN][1000 genomes]
rs1371025	0.95[ASN][1000 genomes]
rs1438819	0.89[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs1438820	0.93[ASN][1000 genomes]
rs1438822	0.92[ASN][1000 genomes]
rs1438827	0.92[ASN][1000 genomes]
rs16901963	0.95[ASN][1000 genomes]
rs16901964	0.92[ASN][1000 genomes]
rs16901965	0.94[ASN][1000 genomes]
rs16901989	0.92[ASN][1000 genomes]
rs16901990	0.95[ASN][1000 genomes]
rs1821934	0.92[ASN][1000 genomes]
rs1866406	0.97[ASN][1000 genomes]
rs2083243	0.95[ASN][1000 genomes]
rs2118764	0.92[ASN][1000 genomes]
rs2165008	0.97[ASN][1000 genomes]
rs2330572	0.85[ASN][1000 genomes]
rs2330619	0.85[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs2330620	0.95[ASN][1000 genomes]
rs2877172	0.91[ASN][1000 genomes]
rs34501299	0.86[ASN][1000 genomes]
rs3747479	0.97[ASN][1000 genomes]
rs3761648	0.97[ASN][1000 genomes]
rs3761649	0.97[ASN][1000 genomes]
rs3761650	0.97[ASN][1000 genomes]
rs4129642	0.87[ASN][1000 genomes]
rs4329028	0.88[ASN][1000 genomes]
rs4395640	0.91[ASN][1000 genomes]
rs4412123	0.86[ASN][1000 genomes]
rs4457088	0.88[ASN][1000 genomes]
rs4457089	0.97[ASN][1000 genomes]
rs4518409	0.86[ASN][1000 genomes]
rs4596389	0.95[ASN][1000 genomes]
rs4642377	0.86[ASN][1000 genomes]
rs4866783	0.88[ASN][1000 genomes]
rs4866784	0.86[ASN][1000 genomes]
rs4866920	0.88[ASN][1000 genomes]
rs57300972	0.86[ASN][1000 genomes]
rs6451772	0.88[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs6451774	0.89[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs6451775	0.83[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs6451781	0.92[ASN][1000 genomes]
rs67274820	0.95[ASN][1000 genomes]
rs6859157	0.95[ASN][1000 genomes]
rs6867533	0.92[ASN][1000 genomes]
rs6868232	0.85[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs6868779	0.86[ASN][1000 genomes]
rs6870136	0.88[ASN][1000 genomes]
rs6871820	0.88[ASN][1000 genomes]
rs6872254	0.94[ASN][1000 genomes]
rs6875933	0.95[ASN][1000 genomes]
rs6881563	0.88[ASN][1000 genomes]
rs6894324	0.89[ASN][1000 genomes]
rs6896350	0.94[ASN][1000 genomes]
rs6896417	0.93[ASN][1000 genomes]
rs71610376	0.93[ASN][1000 genomes]
rs727304	0.89[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs727305	0.87[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs729599	0.95[ASN][1000 genomes]
rs7380559	0.92[ASN][1000 genomes]
rs7449277	0.91[ASN][1000 genomes]
rs7703059	0.94[ASN][1000 genomes]
rs7705343	0.86[ASN][1000 genomes]
rs7708506	0.88[ASN][1000 genomes]
rs7710952	0.88[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs7710978	0.88[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs7711136	0.93[ASN][1000 genomes]
rs7711697	0.92[ASN][1000 genomes]
rs7712949	0.94[ASN][1000 genomes]
rs7715731	0.95[ASN][1000 genomes]
rs7716571	0.93[ASN][1000 genomes]
rs7717459	0.97[ASN][1000 genomes]
rs7720787	0.93[ASN][1000 genomes]
rs7728431	0.85[ASN][1000 genomes]
rs7730841	0.93[ASN][1000 genomes]
rs7736952	0.91[ASN][1000 genomes]
rs7737491	0.86[ASN][1000 genomes]
rs9292913	0.88[ASN][1000 genomes]
rs9292914	0.88[ASN][1000 genomes]
rs9292915	0.88[ASN][1000 genomes]
rs930394	0.94[ASN][1000 genomes]
rs9637783	0.97[ASN][1000 genomes]
rs9637796	0.87[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs9637797	0.87[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs969679	0.97[ASN][1000 genomes]
rs9790879	0.85[ASN][1000 genomes]
rs9790896	0.85[ASN][1000 genomes]
rs9791056	0.88[ASN][1000 genomes]
rs9791059	0.86[ASN][1000 genomes]
rs9791164	0.88[ASN][1000 genomes]
rs987394	0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830279	chr5:44688175-44860815	Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
2	nsv1027897	chr5:44695278-45061623	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
3	nsv597933	chr5:44740989-44810740	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	n/a
4	nsv880712	chr5:44777878-44842260	Strong transcription Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
5	nsv881564	chr5:44783255-44914579	Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
6	nsv881629	chr5:44796042-44836788	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
7	nsv881184	chr5:44796042-44842260	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
8	nsv881280	chr5:44800665-44821736	Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	n/a
9	nsv880618	chr5:44800665-44836788	Strong transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
10	nsv881418	chr5:44800665-44869100	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
11	nsv880397	chr5:44800665-44939293	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10462082	LOC647121	Cis_chr	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:44794200-44808600	Weak transcription	Aorta	Aorta
2	chr5:44799200-44806800	Weak transcription	Dnd41	blood
3	chr5:44800800-44801200	Weak transcription	Hela-S3	cervix

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