Variant report

Variant	rs10470501
Chromosome Location	chr3:101630497-101630498
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1081574	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1081576	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1088047	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1091320	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1378838	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1513118	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1672380	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1672386	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1707608	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1707613	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1707618	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1707619	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs28542140	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2860329	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2925323	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2925325	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2925326	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs797866	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9834402	0.85[ASN][1000 genomes]
rs9844218	0.82[ASN][1000 genomes]
rs9869373	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9881690	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv497784	chr3:101315009-102092989	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	esv3351469	chr3:101511702-101866448	Weak transcription Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv1010762	chr3:101584836-101803821	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:101621200-101633600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr3:101621600-101632800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr3:101623000-101631400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr3:101623000-101631400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr3:101623000-101632200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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