Variant report

Variant	rs3087782
Chromosome Location	chr8:86360773-86360774
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:86360412..86362696-chr8:87043331..87045552,2	MCF-7	breast:

Extended variants
information (count: 95 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs10088136	0.88[ASN][1000 genomes]
rs10095352	0.95[JPT][hapmap];0.80[ASN][1000 genomes]
rs10111039	0.80[ASN][1000 genomes]
rs10504812	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10504813	0.86[CEU][hapmap];0.91[CHB][hapmap];0.87[CHD][hapmap];0.88[GIH][hapmap];0.95[JPT][hapmap];0.92[MEX][hapmap];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10907474	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs11261471	0.82[JPT][hapmap]
rs11261474	0.95[JPT][hapmap]
rs11780285	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11985733	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs12541445	0.82[JPT][hapmap]
rs12544332	0.86[JPT][hapmap]
rs1303806	0.91[JPT][hapmap]
rs13252971	0.95[JPT][hapmap]
rs13255540	0.84[ASN][1000 genomes]
rs13259399	0.86[JPT][hapmap]
rs1389245	0.85[ASN][1000 genomes]
rs1389247	0.85[ASN][1000 genomes]
rs1390711	0.91[JPT][hapmap]
rs1472360	0.82[ASN][1000 genomes]
rs1493302	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs1496526	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1496527	0.81[EUR][1000 genomes]
rs1496529	0.95[JPT][hapmap]
rs1496530	0.95[JPT][hapmap]
rs1496531	0.86[JPT][hapmap]
rs1496532	0.86[JPT][hapmap]
rs1532423	1.00[JPT][hapmap]
rs1532424	0.95[JPT][hapmap]
rs1553015	0.91[JPT][hapmap]
rs16913721	0.86[JPT][hapmap]
rs17042	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1845253	0.94[ASN][1000 genomes]
rs1995056	0.86[JPT][hapmap]
rs1995057	0.82[JPT][hapmap]
rs1995058	0.91[JPT][hapmap]
rs2006767	0.86[JPT][hapmap]
rs2055077	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs20571	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs2072696	0.95[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2279701	0.82[JPT][hapmap]
rs2291787	0.82[JPT][hapmap]
rs2307075	0.95[JPT][hapmap];0.80[ASN][1000 genomes]
rs2403104	0.91[JPT][hapmap]
rs2403105	0.84[ASN][1000 genomes]
rs2453868	0.81[ASN][1000 genomes]
rs2548281	0.95[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs2645047	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2645049	0.85[CEU][hapmap];0.90[CHB][hapmap];0.93[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.84[MKK][hapmap];0.94[TSI][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2645053	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs359535	0.89[CHD][hapmap];0.83[MEX][hapmap]
rs3758076	0.95[JPT][hapmap]
rs3758077	0.80[ASN][1000 genomes]
rs3758078	0.90[CHB][hapmap];0.98[CHD][hapmap];0.90[JPT][hapmap];0.95[ASN][1000 genomes]
rs3808539	0.91[JPT][hapmap]
rs4566	0.82[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs4739700	0.86[JPT][hapmap]
rs4740049	0.91[JPT][hapmap]
rs4740053	0.89[CHD][hapmap]
rs55641432	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs55929157	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58958691	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs66498753	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs67824746	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6988475	0.95[JPT][hapmap];0.80[ASN][1000 genomes]
rs6993387	0.86[JPT][hapmap]
rs6997458	1.00[JPT][hapmap]
rs7001359	0.82[JPT][hapmap]
rs7008772	0.86[JPT][hapmap]
rs7011926	0.91[JPT][hapmap]
rs7016369	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs703	0.91[ASN][1000 genomes]
rs713488	0.85[ASN][1000 genomes]
rs713489	0.85[ASN][1000 genomes]
rs725605	0.90[JPT][hapmap]
rs7386162	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7818163	0.86[JPT][hapmap]
rs903895	0.91[JPT][hapmap]
rs903896	0.91[JPT][hapmap]
rs903897	0.91[JPT][hapmap]
rs9286249	0.80[ASN][1000 genomes]
rs931505	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs9329911	0.87[ASN][1000 genomes]
rs955007	0.80[ASN][1000 genomes]
rs9969643	0.82[CHB][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs9987281	0.82[CHB][hapmap];0.95[JPT][hapmap]
rs999466	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[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	nsv1018483	chr8:86142258-86547831	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS 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	23 gene(s)	inside rSNPs	diseases
2	nsv1024759	chr8:86162507-86361533	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv539659	chr8:86162507-86361533	Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv1022463	chr8:86257031-86547831	Enhancers Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	esv1804888	chr8:86263098-86986703	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	nsv831377	chr8:86263107-86444141	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
7	nsv1028148	chr8:86310570-86553130	Flanking Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
8	esv2761206	chr8:86310582-86468868	Enhancers Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs3087782	C8orf59	cis	cerebellum	SCAN
rs3087782	C8orf59	Cis_1M	lymphoblastoid	RTeQTL
rs3087782	C8orf59	cis	parietal	SCAN

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86351200-86364800	Weak transcription	Liver	Liver
2	chr8:86351200-86367200	Weak transcription	Left Ventricle	heart
3	chr8:86351200-86374000	Weak transcription	Fetal Intestine Small	intestine
4	chr8:86351400-86361800	Weak transcription	Ovary	ovary
5	chr8:86351600-86365200	Weak transcription	Brain Anterior Caudate	brain
6	chr8:86351600-86368200	Weak transcription	Brain Cingulate Gyrus	brain
7	chr8:86353800-86362000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr8:86354400-86362600	Weak transcription	Fetal Muscle Leg	muscle
9	chr8:86354400-86375400	Weak transcription	Psoas Muscle	Psoas
10	chr8:86355200-86361800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr8:86355200-86365200	Weak transcription	Stomach Mucosa	stomach
12	chr8:86358400-86375600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:86358800-86365000	Weak transcription	Fetal Lung	lung
14	chr8:86360000-86363600	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr8:86360400-86363200	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr8:86360400-86366000	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr8:86360600-86363200	Weak transcription	Fetal Intestine Large	intestine
18	chr8:86360600-86364400	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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