Variant report

Variant	rs10113088
Chromosome Location	chr8:114704437-114704438
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 61 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10088339	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs10089522	0.82[ASN][1000 genomes]
rs10097628	0.82[ASN][1000 genomes]
rs10103736	0.81[ASN][1000 genomes]
rs10104685	0.83[ASN][1000 genomes]
rs10105039	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10105221	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10113605	0.81[ASN][1000 genomes]
rs10505206	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10505207	0.83[ASN][1000 genomes]
rs10955672	0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12155931	0.82[ASN][1000 genomes]
rs12386865	0.98[ASN][1000 genomes]
rs12386964	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12547452	0.83[ASN][1000 genomes]
rs12677871	0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12681503	0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs13439326	0.85[ASN][1000 genomes]
rs1377230	0.86[ASN][1000 genomes]
rs1597862	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16884999	0.83[ASN][1000 genomes]
rs16885055	0.82[ASN][1000 genomes]
rs2123383	0.82[ASN][1000 genomes]
rs2123384	0.82[ASN][1000 genomes]
rs2123385	0.83[ASN][1000 genomes]
rs28477627	0.89[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs28529276	0.83[ASN][1000 genomes]
rs28579378	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28673187	0.82[ASN][1000 genomes]
rs28685235	0.83[ASN][1000 genomes]
rs28825376	0.88[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs3911267	0.83[ASN][1000 genomes]
rs4876312	0.82[ASN][1000 genomes]
rs4876315	0.83[ASN][1000 genomes]
rs4876525	0.82[ASN][1000 genomes]
rs4876526	0.82[ASN][1000 genomes]
rs4876527	0.82[ASN][1000 genomes]
rs4876528	0.82[ASN][1000 genomes]
rs4876529	0.84[ASN][1000 genomes]
rs4876531	0.83[ASN][1000 genomes]
rs4876532	0.84[ASN][1000 genomes]
rs62522065	0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs62522112	0.82[ASN][1000 genomes]
rs7014123	0.83[ASN][1000 genomes]
rs734622	0.80[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7461949	0.85[ASN][1000 genomes]
rs7813991	0.82[ASN][1000 genomes]
rs7814054	0.81[ASN][1000 genomes]
rs7816794	0.82[ASN][1000 genomes]
rs7826236	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7826446	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7833423	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9297505	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv817379	chr8:114338391-115011632	Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv818650	chr8:114574863-115477600	Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	esv2758168	chr8:114575703-115321957	Enhancers Transcr. at gene 5' and 3' Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	esv2759636	chr8:114575703-115321957	Active TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv891335	chr8:114589007-114725064	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv891336	chr8:114667112-114753522	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv1851155	chr8:114673166-114773729	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3327619	chr8:114698979-114741570	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:114703400-114704800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr8:114703600-114704800	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr8:114703600-114705000	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr8:114704200-114704600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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