Variant report

Variant	rs55864145
Chromosome Location	chr10:45853664-45853665
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 108 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:104)

rs_ID	r²[population]
rs10900212	0.95[ASN][1000 genomes]
rs11239486	0.94[ASN][1000 genomes]
rs11239491	0.98[ASN][1000 genomes]
rs11239492	0.95[ASN][1000 genomes]
rs11239497	0.95[ASN][1000 genomes]
rs11239505	0.91[ASN][1000 genomes]
rs11511619	0.98[ASN][1000 genomes]
rs11511620	0.95[ASN][1000 genomes]
rs11517281	0.98[ASN][1000 genomes]
rs11523408	0.98[ASN][1000 genomes]
rs12354712	0.95[ASN][1000 genomes]
rs12354742	0.95[ASN][1000 genomes]
rs12354994	0.88[ASN][1000 genomes]
rs12356109	0.98[ASN][1000 genomes]
rs12356140	0.89[ASN][1000 genomes]
rs12358647	0.89[ASN][1000 genomes]
rs12359299	0.96[ASN][1000 genomes]
rs12359302	0.95[ASN][1000 genomes]
rs12360250	0.95[ASN][1000 genomes]
rs12761961	0.88[EUR][1000 genomes]
rs12762303	0.98[ASN][1000 genomes]
rs12763738	0.98[ASN][1000 genomes]
rs12764778	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12768010	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12774369	0.95[ASN][1000 genomes]
rs12783095	0.95[ASN][1000 genomes]
rs12783182	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12783895	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs17157728	0.95[ASN][1000 genomes]
rs17157733	0.93[ASN][1000 genomes]
rs17157736	0.95[ASN][1000 genomes]
rs1864412	0.97[ASN][1000 genomes]
rs1864413	0.98[ASN][1000 genomes]
rs1864414	0.98[ASN][1000 genomes]
rs2082108	0.99[ASN][1000 genomes]
rs2099170	1.00[ASN][1000 genomes]
rs2303885	0.91[ASN][1000 genomes]
rs2310776	0.95[ASN][1000 genomes]
rs28395865	0.94[ASN][1000 genomes]
rs34297550	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs34462692	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34929604	0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs34998367	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35001574	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35267934	0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35300270	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35555369	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35745197	0.91[EUR][1000 genomes]
rs35906360	0.99[ASN][1000 genomes]
rs3780894	0.95[ASN][1000 genomes]
rs3780896	0.95[ASN][1000 genomes]
rs3780897	0.95[ASN][1000 genomes]
rs3780898	0.95[ASN][1000 genomes]
rs3780899	0.95[ASN][1000 genomes]
rs3824613	0.95[ASN][1000 genomes]
rs4986832	0.98[ASN][1000 genomes]
rs4987105	0.98[ASN][1000 genomes]
rs4987106	0.94[ASN][1000 genomes]
rs55717607	0.98[ASN][1000 genomes]
rs55787481	0.94[ASN][1000 genomes]
rs55965812	0.99[ASN][1000 genomes]
rs55978138	0.99[ASN][1000 genomes]
rs55986122	0.99[ASN][1000 genomes]
rs56150414	0.97[ASN][1000 genomes]
rs56180358	0.98[ASN][1000 genomes]
rs57063108	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57398542	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs58167894	0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs58238740	0.95[ASN][1000 genomes]
rs58901177	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs59514896	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs60146827	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs60842538	0.95[ASN][1000 genomes]
rs6413416	0.98[ASN][1000 genomes]
rs6593478	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6593482	0.98[ASN][1000 genomes]
rs66489870	0.98[ASN][1000 genomes]
rs67008983	0.97[ASN][1000 genomes]
rs67491417	0.95[ASN][1000 genomes]
rs7071714	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7077891	0.95[ASN][1000 genomes]
rs7080897	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7081004	0.98[ASN][1000 genomes]
rs7083500	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7084793	0.98[ASN][1000 genomes]
rs7085205	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7093687	0.98[ASN][1000 genomes]
rs7097429	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs71494771	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs71494772	0.86[ASN][1000 genomes]
rs71494775	0.98[ASN][1000 genomes]
rs71494776	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs71494779	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72561472	0.94[ASN][1000 genomes]
rs745986	0.91[ASN][1000 genomes]
rs7896861	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7898465	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7909740	0.98[ASN][1000 genomes]
rs7909768	0.98[ASN][1000 genomes]
rs7913488	0.98[ASN][1000 genomes]
rs7917687	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7919239	0.80[ASN][1000 genomes]
rs7921503	0.98[ASN][1000 genomes]
rs9663661	0.98[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	nsv895105	chr10:45636867-45928822	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv430166	chr10:45668894-46148794	Bivalent Enhancer Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv993428	chr10:45742877-46224333	Enhancers Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv895107	chr10:45850300-45953767	Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45848400-45863400	Weak transcription	Primary B cells from cord blood	blood
2	chr10:45850000-45857800	Weak transcription	Primary B cells from peripheral blood	blood
3	chr10:45850400-45857600	Weak transcription	K562	blood
4	chr10:45852000-45854200	Weak transcription	Thymus	Thymus
5	chr10:45852400-45854200	Weak transcription	Fetal Thymus	thymus

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