Variant report

Variant	rs7013824
Chromosome Location	chr8:39808425-39808426
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:62)

rs_ID	r²[population]
rs10085935	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10113563	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10216901	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10504013	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10755980	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10958573	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10958574	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11773909	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11773975	0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11777082	0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11779313	0.83[EUR][1000 genomes]
rs11779697	0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11779700	0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11781217	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11786337	0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11787388	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11787449	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11992749	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11994259	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2052377	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2052379	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2111741	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2160860	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2340952	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2543042	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2543044	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2543046	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2543047	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2543049	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2543050	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2729456	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2729459	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2729460	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2729462	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2729476	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs28841363	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35995308	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3739319	0.86[EUR][1000 genomes]
rs55698142	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55818481	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55992954	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56045817	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56838465	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59312250	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59445010	0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62512638	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6474194	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6474195	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6474196	0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6474197	0.84[ASN][1000 genomes]
rs6983463	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6983940	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6984887	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7000868	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7003411	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7824841	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7828760	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7832080	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7839881	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7839885	0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7845003	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7845418	0.91[EUR][1000 genomes];0.97[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:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39797800-39808800	Weak transcription	Left Ventricle	heart
2	chr8:39802800-39808800	Weak transcription	Lung	lung
3	chr8:39803400-39809200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr8:39804400-39809200	Enhancers	Primary B cells from peripheral blood	blood
5	chr8:39805000-39809800	Enhancers	Primary hematopoietic stem cells short term culture	blood
6	chr8:39805400-39810200	Enhancers	Primary hematopoietic stem cells	blood
7	chr8:39805600-39808600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr8:39805600-39809200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr8:39806000-39817000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr8:39806200-39810000	Active TSS	Liver	Liver
11	chr8:39807000-39809400	Weak transcription	A549	lung
12	chr8:39807200-39809000	Enhancers	Primary neutrophils fromperipheralblood	blood
13	chr8:39807600-39808800	Weak transcription	K562	blood
14	chr8:39807600-39809000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:39807600-39809000	Enhancers	GM12878-XiMat	blood
16	chr8:39807600-39809600	Enhancers	Primary B cells from cord blood	blood
17	chr8:39807800-39808600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr8:39807800-39809200	Enhancers	Placenta	Placenta
19	chr8:39808000-39808800	Enhancers	H9 Cell Line	embryonic stem cell
20	chr8:39808000-39808800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr8:39808200-39808800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr8:39808200-39809800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
23	chr8:39808400-39808800	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr8:39808400-39809200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr8:39808400-39809400	Enhancers	Rectal Mucosa Donor 29	rectum

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