Variant report

Variant	rs13251920
Chromosome Location	chr8:122905905-122905906
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs13280949	0.99[EUR][1000 genomes]
rs16893010	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs16896378	1.00[CEU][hapmap];0.87[JPT][hapmap];0.80[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs16896381	0.99[EUR][1000 genomes]
rs34167945	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34800699	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35721900	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs55781842	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61194912	0.82[AMR][1000 genomes]
rs6470048	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6981419	0.85[ASN][1000 genomes]
rs9643167	0.99[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	esv2752207	chr8:122869651-122961848	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a
2	nsv465795	chr8:122895259-123009699	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv612133	chr8:122895259-123009699	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:122899200-122906000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:122904600-122906600	Enhancers	HUVEC	blood vessel
3	chr8:122905400-122906600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr8:122905400-122906800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr8:122905400-122906800	Enhancers	Osteobl	bone
6	chr8:122905600-122906200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr8:122905600-122906800	Enhancers	HSMMtube	muscle
8	chr8:122905800-122906000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr8:122905800-122906400	Enhancers	HMEC	breast
10	chr8:122905800-122906400	Enhancers	HSMM	muscle
11	chr8:122905800-122906400	Enhancers	NH-A	brain
12	chr8:122905800-122906600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr8:122905800-122906600	Enhancers	Muscle Satellite Cultured Cells	--
14	chr8:122905800-122906600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr8:122905800-122906600	Enhancers	NHDF-Ad	bronchial
16	chr8:122905800-122906600	Enhancers	NHLF	lung

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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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