Variant report

Variant	rs10104658
Chromosome Location	chr8:122241631-122241632
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10089470	0.95[EUR][1000 genomes]
rs10090549	0.94[EUR][1000 genomes]
rs10090684	0.94[EUR][1000 genomes]
rs10100820	0.95[EUR][1000 genomes]
rs10100931	0.95[EUR][1000 genomes]
rs10101120	0.95[EUR][1000 genomes]
rs10102893	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10103819	0.94[EUR][1000 genomes]
rs10104288	0.94[EUR][1000 genomes]
rs10104487	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10104851	0.95[EUR][1000 genomes]
rs10107769	0.95[EUR][1000 genomes]
rs10112656	0.94[EUR][1000 genomes]
rs1021897	0.92[EUR][1000 genomes]
rs1021898	0.92[EUR][1000 genomes]
rs1021899	0.92[EUR][1000 genomes]
rs1021900	0.92[EUR][1000 genomes]
rs10505396	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1124090	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11996526	0.92[EUR][1000 genomes]
rs13258658	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13261111	0.95[EUR][1000 genomes]
rs1504650	0.92[EUR][1000 genomes]
rs1504651	0.92[EUR][1000 genomes]
rs1504652	0.92[EUR][1000 genomes]
rs1504653	0.92[EUR][1000 genomes]
rs1504654	0.93[EUR][1000 genomes]
rs1504655	0.93[EUR][1000 genomes]
rs1504656	0.95[EUR][1000 genomes]
rs1553507	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1553508	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17205796	0.92[EUR][1000 genomes]
rs17205915	0.92[EUR][1000 genomes]
rs17265202	0.92[EUR][1000 genomes]
rs17265314	0.92[EUR][1000 genomes]
rs1847545	0.95[EUR][1000 genomes]
rs2134931	0.93[EUR][1000 genomes]
rs2174348	0.92[EUR][1000 genomes]
rs2174349	0.92[EUR][1000 genomes]
rs2202381	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2386064	0.96[EUR][1000 genomes]
rs2386065	0.95[EUR][1000 genomes]
rs34698310	0.91[EUR][1000 genomes]
rs35806375	0.90[EUR][1000 genomes]
rs4870764	0.95[EUR][1000 genomes]
rs57442891	0.81[EUR][1000 genomes]
rs6982766	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6988416	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6988639	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6989776	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7815430	0.85[EUR][1000 genomes]
rs7821650	0.91[EUR][1000 genomes]
rs905759	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][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	nsv891424	chr8:121873345-122393258	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv1844734	chr8:121928250-122283585	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	esv3330574	chr8:122039099-122386130	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv891426	chr8:122078334-122393258	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr8:122240600-122246000	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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