Variant report

Variant	rs73370990
Chromosome Location	chr5:167298653-167298654
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1972621	1.00[AMR][1000 genomes]
rs57053085	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57599895	1.00[AMR][1000 genomes]
rs60201000	1.00[AMR][1000 genomes]
rs60431833	1.00[AMR][1000 genomes]
rs60519985	1.00[AMR][1000 genomes]
rs6865076	1.00[AMR][1000 genomes]
rs73370925	1.00[AMR][1000 genomes]
rs73370952	1.00[AMR][1000 genomes]
rs73370968	1.00[AMR][1000 genomes]
rs73370976	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73370977	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73370980	1.00[AMR][1000 genomes]
rs73370984	1.00[AMR][1000 genomes]
rs73370987	1.00[AMR][1000 genomes]
rs73370988	1.00[AMR][1000 genomes]
rs73370989	0.91[AFR][1000 genomes];1.00[AMR][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	nsv462511	chr5:167275087-167324809	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
2	nsv600254	chr5:167275087-167324809	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:167251800-167299000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:167266600-167326200	Weak transcription	HMEC	breast
3	chr5:167281800-167301600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr5:167285600-167325600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr5:167290200-167301600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:167291800-167300800	Weak transcription	NHEK	skin
7	chr5:167292000-167299800	Weak transcription	Fetal Lung	lung
8	chr5:167296800-167303600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:167298000-167299000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr5:167298000-167299200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr5:167298000-167311000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr5:167298400-167299600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr5:167298600-167299000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

Quick Search:

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

what's new

Quick links