Variant report

Variant	rs16892236
Chromosome Location	chr8:99475572-99475573
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	GATA3	chr8:99475387-99475749	SH-SY5Y	brain:	n/a	n/a

Variant related genes	Relation type
RNU6-748P	TF binding region

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10086870	0.88[CEU][hapmap];0.82[EUR][1000 genomes]
rs10098835	0.83[AMR][1000 genomes]
rs10099978	1.00[CEU][hapmap];0.91[TSI][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10100346	0.92[CEU][hapmap]
rs10100378	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10100546	1.00[CEU][hapmap];0.83[JPT][hapmap];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10100577	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10111264	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10441501	0.81[CEU][hapmap];0.89[TSI][hapmap]
rs10755897	0.83[GIH][hapmap]
rs10955175	0.83[AMR][1000 genomes]
rs10955176	0.96[CEU][hapmap];0.91[TSI][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10955177	0.84[AMR][1000 genomes]
rs10955178	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10955181	0.80[TSI][hapmap]
rs10955184	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10955185	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs11781352	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11985382	1.00[CEU][hapmap];0.91[TSI][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12056323	0.88[CEU][hapmap];0.89[TSI][hapmap];0.80[EUR][1000 genomes]
rs12541026	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12542022	1.00[CEU][hapmap];0.91[CHB][hapmap];0.98[CHD][hapmap];0.89[GIH][hapmap];0.87[JPT][hapmap];0.98[TSI][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12542931	1.00[CEU][hapmap];0.93[TSI][hapmap];0.85[EUR][1000 genomes]
rs12544768	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs12546344	0.90[AFR][1000 genomes]
rs12547922	1.00[CEU][hapmap];0.91[TSI][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12548477	1.00[CEU][hapmap];0.91[TSI][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12549563	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12550198	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs16897061	0.96[CEU][hapmap];0.91[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];0.87[MKK][hapmap];0.95[TSI][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34580087	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs3802198	1.00[CEU][hapmap];0.93[TSI][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4130753	0.81[CEU][hapmap];0.87[TSI][hapmap];0.81[AMR][1000 genomes]
rs4236853	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4301421	1.00[CEU][hapmap];0.93[TSI][hapmap];0.84[EUR][1000 genomes]
rs4332102	1.00[CEU][hapmap];0.93[TSI][hapmap];0.85[EUR][1000 genomes]
rs4370499	0.96[CEU][hapmap];0.91[CHB][hapmap];0.98[CHD][hapmap];0.89[GIH][hapmap];0.87[JPT][hapmap];0.95[TSI][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4388428	0.81[CEU][hapmap];0.87[TSI][hapmap]
rs4442112	0.87[JPT][hapmap]
rs4618666	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4734406	0.81[CEU][hapmap];0.83[JPT][hapmap];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4734407	1.00[CEU][hapmap];0.91[TSI][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4735564	0.88[CEU][hapmap];0.89[TSI][hapmap];0.81[EUR][1000 genomes]
rs4995528	0.81[CEU][hapmap];0.83[JPT][hapmap];0.89[TSI][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs62532757	0.80[EUR][1000 genomes]
rs6651181	0.80[TSI][hapmap]
rs7007360	0.81[CEU][hapmap];0.83[JPT][hapmap];0.89[TSI][hapmap];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7011763	0.84[TSI][hapmap]
rs7015739	1.00[CEU][hapmap];0.93[TSI][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7016626	0.87[JPT][hapmap]
rs7815227	0.81[CEU][hapmap];0.82[AMR][1000 genomes]
rs7845395	1.00[CEU][hapmap];0.93[TSI][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9642951	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032904	chr8:98756076-99476925	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv539687	chr8:98756076-99476925	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv831406	chr8:99290745-99482076	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv1027362	chr8:99469281-99715845	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv539689	chr8:99469281-99715845	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr8:99461800-99525000	Weak transcription	Psoas Muscle	Psoas
2	chr8:99465000-99478600	Weak transcription	HUVEC	blood vessel
3	chr8:99465200-99478800	Weak transcription	A549	lung
4	chr8:99466800-99477200	Weak transcription	Ovary	ovary
5	chr8:99467000-99478600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:99467200-99478600	Weak transcription	NH-A	brain
7	chr8:99467200-99478600	Weak transcription	NHEK	skin
8	chr8:99468000-99476400	Weak transcription	Fetal Heart	heart
9	chr8:99469200-99476400	Weak transcription	HSMM	muscle
10	chr8:99470200-99476000	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr8:99472000-99479200	Weak transcription	HSMMtube	muscle
12	chr8:99472200-99478600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr8:99472400-99476000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr8:99472400-99476200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr8:99472400-99477400	Weak transcription	Placenta	Placenta
16	chr8:99472400-99479000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr8:99472400-99479000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr8:99473600-99475600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr8:99474000-99479200	Weak transcription	Fetal Lung	lung
20	chr8:99474200-99475800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr8:99474200-99478600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr8:99474400-99475600	Enhancers	Osteobl	bone
23	chr8:99474400-99476400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr8:99474600-99478800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr8:99475200-99481000	Enhancers	NHDF-Ad	bronchial

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