Variant report

Variant	rs4703829
Chromosome Location	chr5:80574682-80574683
allele	G/T
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:13)

rs_ID	r²[population]
rs1039326	0.88[EUR][1000 genomes]
rs12653169	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12653916	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12654520	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12657721	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12659947	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs16878586	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4704716	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs56270508	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs57802618	0.80[EUR][1000 genomes]
rs58471723	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs59621118	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61696419	0.88[EUR][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	nsv1024844	chr5:79862428-80860430	Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv598750	chr5:80503528-80599578	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 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	chr5:80554600-80576400	Weak transcription	Pancreas	Pancrea
2	chr5:80565200-80580400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:80566200-80587800	Weak transcription	Ovary	ovary
4	chr5:80566400-80575400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr5:80566400-80581400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr5:80566400-80587600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr5:80566800-80587600	Weak transcription	Right Ventricle	heart
8	chr5:80568000-80585600	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr5:80570400-80587200	Weak transcription	Primary B cells from cord blood	blood
10	chr5:80571600-80583000	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr5:80571800-80579600	Weak transcription	Fetal Heart	heart
12	chr5:80572000-80595200	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr5:80572400-80578800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:80573200-80578600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr5:80573800-80587400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr5:80574600-80585600	Weak transcription	Dnd41	blood

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