Variant report

Variant	rs12386964
Chromosome Location	chr8:114698419-114698420
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10088339	0.87[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs10089522	0.81[ASN][1000 genomes]
rs10097628	0.81[ASN][1000 genomes]
rs10099644	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs10103736	0.80[ASN][1000 genomes]
rs10104685	0.81[ASN][1000 genomes]
rs10105039	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10105221	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10110242	0.81[ASN][1000 genomes]
rs10113088	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10113605	0.80[ASN][1000 genomes]
rs10505206	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10505207	0.85[ASN][1000 genomes]
rs10955672	0.86[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12155931	0.81[ASN][1000 genomes]
rs12386865	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs12542164	0.81[ASN][1000 genomes]
rs12547452	0.81[ASN][1000 genomes]
rs12677871	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12681503	0.98[ASN][1000 genomes]
rs13439326	0.87[ASN][1000 genomes]
rs1377230	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs1597862	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16884999	0.85[ASN][1000 genomes]
rs16885055	0.81[ASN][1000 genomes]
rs2123383	0.81[ASN][1000 genomes]
rs2123384	0.81[ASN][1000 genomes]
rs2123385	0.81[ASN][1000 genomes]
rs28477627	0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs28529276	0.82[ASN][1000 genomes]
rs28579378	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28673187	0.81[ASN][1000 genomes]
rs28685235	0.82[ASN][1000 genomes]
rs28825376	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs3911267	0.82[ASN][1000 genomes]
rs4074797	0.83[CHB][hapmap];0.86[JPT][hapmap]
rs4876312	0.81[ASN][1000 genomes]
rs4876315	0.82[ASN][1000 genomes]
rs4876525	0.81[ASN][1000 genomes]
rs4876526	0.81[ASN][1000 genomes]
rs4876527	0.81[ASN][1000 genomes]
rs4876528	0.81[ASN][1000 genomes]
rs4876529	0.83[ASN][1000 genomes]
rs4876531	0.82[ASN][1000 genomes]
rs4876532	0.83[ASN][1000 genomes]
rs62522065	0.98[ASN][1000 genomes]
rs62522112	0.81[ASN][1000 genomes]
rs7014123	0.81[ASN][1000 genomes]
rs734622	0.88[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7461949	0.87[ASN][1000 genomes]
rs7813991	0.81[ASN][1000 genomes]
rs7814054	0.80[ASN][1000 genomes]
rs7816794	0.83[ASN][1000 genomes]
rs7826236	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7826446	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7833423	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9297505	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:114697400-114698600	Enhancers	Primary B cells from cord blood	blood
2	chr8:114698200-114703400	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr8:114698200-114703600	Weak transcription	Monocytes-CD14+_RO01746	blood

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