Variant report

Variant	rs17635403
Chromosome Location	chr6:117767919-117767920
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10080784	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10081005	0.89[GIH][hapmap]
rs11757765	1.00[JPT][hapmap]
rs11758857	1.00[JPT][hapmap]
rs1321811	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17079193	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17079201	1.00[CHB][hapmap]
rs17079205	1.00[CHB][hapmap]
rs17165	1.00[CHB][hapmap]
rs17573446	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17574179	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17574269	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17635492	1.00[CHB][hapmap]
rs17636252	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17636431	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6913494	0.83[GIH][hapmap]
rs6932793	0.93[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6940229	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72959681	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9320600	0.83[GIH][hapmap]
rs9320601	0.83[GIH][hapmap]
rs9320602	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9320603	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9481717	0.93[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.95[TSI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9481718	0.93[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.95[TSI][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9489188	0.93[CEU][hapmap];1.00[CHB][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9489189	0.93[CEU][hapmap];1.00[CHB][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9489191	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9489192	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9489194	0.93[CEU][hapmap];1.00[CHB][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9489195	0.93[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.95[TSI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9489197	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9489198	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9986462	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532050	chr6:117528154-118203005	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription 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

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:117763000-117772200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr6:117764200-117768200	Weak transcription	NHLF	lung
3	chr6:117766200-117768000	Weak transcription	NHEK	skin
4	chr6:117766200-117768600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr6:117766200-117768600	Weak transcription	Hela-S3	cervix
6	chr6:117766400-117768200	Weak transcription	HMEC	breast
7	chr6:117766400-117769000	Weak transcription	NHDF-Ad	bronchial
8	chr6:117767000-117768000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr6:117767200-117768200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr6:117767400-117768200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:117767400-117768400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr6:117767400-117770800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr6:117767400-117771600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr6:117767600-117769600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr6:117767800-117768000	Enhancers	HSMMtube	muscle
16	chr6:117767800-117768200	Flanking Active TSS	Osteobl	bone
17	chr6:117767800-117768600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
18	chr6:117767800-117769200	Enhancers	A549	lung
19	chr6:117767800-117769200	Enhancers	NH-A	brain
20	chr6:117767800-117769400	Enhancers	HSMM	muscle
21	chr6:117767800-117769600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr6:117767800-117771200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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