Variant report

Variant	rs4610128
Chromosome Location	chr20:11374805-11374806
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs6040600	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6040603	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6040605	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6040608	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6040611	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6040615	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6040618	0.94[AFR][1000 genomes]
rs6040626	0.93[AFR][1000 genomes]
rs6078159	0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6078166	0.88[AFR][1000 genomes]
rs73245659	0.96[AFR][1000 genomes]
rs910259	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs996383	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs996384	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs996385	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1065969	chr20:10850562-11464172	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv544181	chr20:10850562-11464172	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv585415	chr20:11134907-11383327	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv432099	chr20:11371093-11476900	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4610128	FUZ	trans	parietal	SCAN

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:11372200-11375800	Weak transcription	A549	lung
2	chr20:11374000-11376800	Enhancers	HMEC	breast
3	chr20:11374200-11376200	Enhancers	NHEK	skin
4	chr20:11374200-11376600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr20:11374600-11377000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr20:11374800-11376600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr20:11374800-11376600	Enhancers	NH-A	brain
8	chr20:11374800-11376800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr20:11374800-11376800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr20:11374800-11376800	Enhancers	Osteobl	bone

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