Variant report

Variant	rs10881868
Chromosome Location	chr10:92716072-92716073
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 83 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1001845	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1001846	0.87[EUR][1000 genomes]
rs1072491	0.87[EUR][1000 genomes]
rs10736059	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10785977	0.87[EUR][1000 genomes]
rs10785978	0.87[EUR][1000 genomes]
rs10785979	0.87[EUR][1000 genomes]
rs10785980	0.87[EUR][1000 genomes]
rs10785981	0.87[EUR][1000 genomes]
rs10881861	0.87[EUR][1000 genomes]
rs10881864	0.87[EUR][1000 genomes]
rs10881865	0.87[EUR][1000 genomes]
rs10881866	0.87[EUR][1000 genomes]
rs10881867	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10881870	0.86[EUR][1000 genomes]
rs10881871	0.87[EUR][1000 genomes]
rs11186383	0.89[EUR][1000 genomes]
rs11186384	0.87[EUR][1000 genomes]
rs11186385	0.87[EUR][1000 genomes]
rs11186390	0.87[EUR][1000 genomes]
rs11186398	0.87[EUR][1000 genomes]
rs11186399	0.87[EUR][1000 genomes]
rs1122870	0.87[EUR][1000 genomes]
rs11528048	0.87[EUR][1000 genomes]
rs11594833	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11596841	0.87[EUR][1000 genomes]
rs11812869	0.87[EUR][1000 genomes]
rs11814844	0.87[EUR][1000 genomes]
rs12219023	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12250934	0.86[ASN][1000 genomes]
rs12570633	0.87[EUR][1000 genomes]
rs12573344	0.87[EUR][1000 genomes]
rs12772494	0.86[EUR][1000 genomes]
rs12778021	0.87[EUR][1000 genomes]
rs12779258	0.87[EUR][1000 genomes]
rs12780522	0.87[EUR][1000 genomes]
rs1334580	0.87[EUR][1000 genomes]
rs1334582	0.87[EUR][1000 genomes]
rs1418815	0.87[EUR][1000 genomes]
rs1544217	0.87[EUR][1000 genomes]
rs2141375	0.87[EUR][1000 genomes]
rs2420498	0.87[EUR][1000 genomes]
rs28849130	0.87[EUR][1000 genomes]
rs3885867	0.87[EUR][1000 genomes]
rs3885868	0.87[EUR][1000 genomes]
rs3981165	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4397747	0.87[EUR][1000 genomes]
rs4411211	0.87[EUR][1000 genomes]
rs4423105	0.87[EUR][1000 genomes]
rs4439428	0.82[EUR][1000 genomes]
rs4553280	0.87[EUR][1000 genomes]
rs4639845	0.87[EUR][1000 genomes]
rs4639846	0.87[EUR][1000 genomes]
rs4933624	0.81[ASN][1000 genomes]
rs4933626	0.86[ASN][1000 genomes]
rs4933627	0.87[EUR][1000 genomes]
rs4933630	0.87[EUR][1000 genomes]
rs4933632	0.87[EUR][1000 genomes]
rs6583740	0.87[EUR][1000 genomes]
rs6583741	0.87[EUR][1000 genomes]
rs7067705	0.87[EUR][1000 genomes]
rs7071167	0.87[EUR][1000 genomes]
rs7071323	0.87[EUR][1000 genomes]
rs7071533	0.87[EUR][1000 genomes]
rs7075411	0.87[EUR][1000 genomes]
rs7079028	0.87[EUR][1000 genomes]
rs7083495	0.87[EUR][1000 genomes]
rs7093432	0.87[EUR][1000 genomes]
rs7095281	0.86[EUR][1000 genomes]
rs7099297	0.87[EUR][1000 genomes]
rs7099420	0.87[EUR][1000 genomes]
rs7099639	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7099671	0.87[EUR][1000 genomes]
rs7895456	0.87[EUR][1000 genomes]
rs7896199	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7897141	0.87[EUR][1000 genomes]
rs7897403	0.87[EUR][1000 genomes]
rs7897603	0.87[EUR][1000 genomes]
rs7897624	0.87[EUR][1000 genomes]
rs7906208	0.86[EUR][1000 genomes]
rs9664170	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831945	chr10:92590576-92793582	Active TSS Enhancers Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	esv19293	chr10:92708763-92723506	Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:92707600-92719400	Weak transcription	HMEC	breast
2	chr10:92707800-92719200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr10:92714800-92716800	ZNF genes & repeats	Dnd41	blood
4	chr10:92714800-92717200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr10:92715200-92737000	Weak transcription	Thymus	Thymus
6	chr10:92715400-92717600	Strong transcription	Fetal Thymus	thymus

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