Variant report

Variant	rs11001729
Chromosome Location	chr10:54111895-54111896
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10508971	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11001698	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11001726	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11001728	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11812118	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11815399	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12767827	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12775601	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12776422	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12778940	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12780421	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1528873	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1528874	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1528877	0.84[CEU][hapmap]
rs1569198	0.84[CEU][hapmap];0.86[JPT][hapmap]
rs1569199	0.84[CEU][hapmap];0.86[JPT][hapmap]
rs1863730	0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7908091	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[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	nsv532194	chr10:53746620-54735550	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv895399	chr10:53900872-54219820	Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:54103800-54113600	Weak transcription	A549	lung
2	chr10:54107600-54113000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr10:54109400-54114000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr10:54110800-54112600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr10:54111000-54112200	Enhancers	Osteobl	bone
6	chr10:54111200-54112400	Enhancers	HUVEC	blood vessel
7	chr10:54111200-54114400	Enhancers	Muscle Satellite Cultured Cells	--
8	chr10:54111200-54114400	Enhancers	HMEC	breast
9	chr10:54111200-54114400	Enhancers	HSMM	muscle
10	chr10:54111600-54112400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr10:54111600-54112400	Enhancers	NHEK	skin
12	chr10:54111800-54112000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr10:54111800-54113000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr10:54111800-54113600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr10:54111800-54114000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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