Variant report

Variant	rs59445010
Chromosome Location	chr8:39798597-39798598
allele	C/T
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:62)

rs_ID	r²[population]
rs10085935	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10113563	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10216901	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10504013	0.96[EUR][1000 genomes]
rs10755980	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10958573	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10958574	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11773909	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11773975	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11777082	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11779313	0.89[EUR][1000 genomes]
rs11779697	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11779700	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11781217	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11786337	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11787388	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11787449	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11992749	0.96[EUR][1000 genomes]
rs11994259	0.96[EUR][1000 genomes]
rs2052377	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2052379	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2111741	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2160860	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2340952	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2543042	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2543044	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2543046	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2543047	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2543049	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2543050	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2729456	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2729459	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2729460	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2729462	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2729476	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28841363	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35995308	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3739319	0.92[EUR][1000 genomes]
rs55698142	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55818481	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55992954	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56045817	0.93[EUR][1000 genomes]
rs56838465	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59312250	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62512638	0.91[EUR][1000 genomes]
rs6474194	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6474195	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6474196	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6474197	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6983463	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6983940	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6984887	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7000868	0.94[EUR][1000 genomes]
rs7003411	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7013824	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7824841	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7828760	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7832080	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7839881	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7839885	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7845003	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7845418	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][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	nsv539555	chr8:39683857-40673606	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1033371	chr8:39749437-39899540	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39785600-39805800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr8:39793400-39798600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr8:39794400-39801600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr8:39796600-39806200	Weak transcription	Small Intestine	intestine
5	chr8:39797800-39798600	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr8:39797800-39798800	Enhancers	Primary hematopoietic stem cells	blood
7	chr8:39797800-39799000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr8:39797800-39799400	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr8:39797800-39799600	Weak transcription	Right Atrium	heart
10	chr8:39797800-39800000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr8:39797800-39800600	Weak transcription	Primary B cells from cord blood	blood
12	chr8:39797800-39802200	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr8:39797800-39802400	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr8:39797800-39802800	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr8:39797800-39803000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr8:39797800-39805800	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr8:39797800-39808400	Weak transcription	Fetal Lung	lung
18	chr8:39797800-39808800	Weak transcription	Left Ventricle	heart
19	chr8:39798000-39799000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr8:39798000-39800600	Weak transcription	GM12878-XiMat	blood
21	chr8:39798000-39801400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr8:39798000-39805600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr8:39798200-39798600	Weak transcription	Hela-S3	cervix
24	chr8:39798200-39799800	Weak transcription	HUVEC	blood vessel
25	chr8:39798200-39801200	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr8:39798200-39801400	Weak transcription	Duodenum Mucosa	Duodenum
27	chr8:39798200-39801600	Enhancers	A549	lung
28	chr8:39798200-39805600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr8:39798400-39799600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr8:39798400-39800600	Weak transcription	Primary B cells from peripheral blood	blood
31	chr8:39798400-39801200	Weak transcription	K562	blood

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