Variant report

Variant	rs8060611
Chromosome Location	chr16:12046165-12046166
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:12044743..12047515-chr16:12054722..12057306,2	K562	blood:
2	chr16:12012124..12014555-chr16:12045355..12047902,2	K562	blood:

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10451099	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10468251	0.91[ASN][1000 genomes]
rs10852345	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10852346	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11075035	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11075036	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11075037	0.91[ASN][1000 genomes]
rs11570137	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11570173	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11864397	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12597378	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12926535	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12927256	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12928141	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12929036	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12929544	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12929852	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12933691	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12934607	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2017662	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35965279	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs365423	0.87[ASN][1000 genomes]
rs366262	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3743591	0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3851002	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3851003	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs387871	0.88[ASN][1000 genomes]
rs3916675	0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57171695	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58398910	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59320000	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6498255	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6498256	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6498257	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7189024	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7190636	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7191310	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7195514	0.96[ASN][1000 genomes]
rs72782778	0.96[ASN][1000 genomes]
rs8046211	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8047277	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8051343	0.95[ASN][1000 genomes]
rs8055129	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8062121	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9922422	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9922795	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[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	nsv1042660	chr16:11846873-12110435	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv571458	chr16:11925008-12087282	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	nsv905347	chr16:12010444-12243329	Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	esv3379697	chr16:12011449-12049700	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv1043096	chr16:12013915-12840769	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
6	nsv482458	chr16:12014925-12145977	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
7	nsv1043959	chr16:12039346-12285269	Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12040400-12065400	Weak transcription	Fetal Intestine Small	intestine
2	chr16:12042000-12049200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr16:12042000-12049600	Weak transcription	A549	lung
4	chr16:12042200-12064400	Weak transcription	Fetal Stomach	stomach
5	chr16:12043200-12049200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr16:12044600-12047400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr16:12044600-12049400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr16:12044800-12046400	Weak transcription	HepG2	liver
9	chr16:12044800-12048000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr16:12044800-12048800	Weak transcription	NHDF-Ad	bronchial
11	chr16:12044800-12049000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr16:12044800-12049200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr16:12044800-12052400	Weak transcription	GM12878-XiMat	blood
14	chr16:12044800-12056400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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