Variant report

Variant	rs72689116
Chromosome Location	chr14:85762769-85762770
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12436591	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12436824	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17201916	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs60463145	0.92[EUR][1000 genomes]
rs6574813	0.91[EUR][1000 genomes]
rs7140796	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7159595	0.82[EUR][1000 genomes]
rs72689118	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72689121	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72689126	0.92[EUR][1000 genomes]
rs72689127	0.92[EUR][1000 genomes]
rs895911	0.87[EUR][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	esv2422273	chr14:85703149-85767292	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:85759200-85763800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr14:85762000-85763800	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr14:85762200-85763200	Enhancers	HUVEC	blood vessel
4	chr14:85762200-85763400	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr14:85762400-85763800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr14:85762600-85763200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr14:85762600-85763200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr14:85762600-85763200	Enhancers	Osteobl	bone
9	chr14:85762600-85763400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr14:85762600-85763400	Enhancers	Primary hematopoietic stem cells short term culture	blood
11	chr14:85762600-85763400	Enhancers	HSMM	muscle
12	chr14:85762600-85763600	Enhancers	Primary hematopoietic stem cells	blood

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Input of quick search could be:

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

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