Variant report

Variant	rs845133
Chromosome Location	chr10:90410292-90410293
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10749594	0.89[ASN][1000 genomes]
rs10788608	0.87[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs10788610	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10887837	0.84[CHB][hapmap];0.95[JPT][hapmap]
rs10887839	0.90[CEU][hapmap];0.92[CHB][hapmap];0.95[JPT][hapmap]
rs10887840	0.94[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap]
rs10887841	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs10887843	0.85[ASN][1000 genomes]
rs11202781	0.94[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs1409137	0.90[CEU][hapmap];0.92[CHB][hapmap];0.90[JPT][hapmap]
rs1555841	0.83[CHB][hapmap];0.93[JPT][hapmap]
rs1769686	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1934447	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1980811	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2274312	0.83[CHB][hapmap];0.95[JPT][hapmap]
rs2296545	0.84[CHB][hapmap];0.95[JPT][hapmap]
rs2576168	0.90[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap]
rs2576178	0.94[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs2765446	0.95[CEU][hapmap];0.95[CHB][hapmap];0.89[JPT][hapmap]
rs2765452	0.89[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap]
rs701826	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7476392	0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs750507	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7912280	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948664	chr10:90076715-90517150	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv529324	chr10:90198865-90738588	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
3	nsv430254	chr10:90265420-90500520	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv1044680	chr10:90316066-90466092	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv540740	chr10:90316066-90466092	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv551839	chr10:90334835-90422136	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90402800-90410800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr10:90402800-90417600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr10:90407000-90415000	Weak transcription	Gastric	stomach
4	chr10:90408800-90411800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr10:90409000-90417800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr10:90409400-90410600	Weak transcription	HMEC	breast
7	chr10:90409800-90413200	Enhancers	Hela-S3	cervix
8	chr10:90410000-90410400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr10:90410000-90410800	Enhancers	A549	lung
10	chr10:90410000-90410800	Enhancers	NHLF	lung
11	chr10:90410000-90411800	Enhancers	NHEK	skin
12	chr10:90410000-90412800	Enhancers	HUVEC	blood vessel
13	chr10:90410000-90413000	Enhancers	Muscle Satellite Cultured Cells	--
14	chr10:90410000-90413000	Enhancers	NH-A	brain
15	chr10:90410000-90413200	Enhancers	NHDF-Ad	bronchial
16	chr10:90410200-90411200	Enhancers	HSMM	muscle
17	chr10:90410200-90413000	Enhancers	Osteobl	bone
18	chr10:90410200-90413200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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