Variant report

Variant	rs566827
Chromosome Location	chr22:27720124-27720125
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12158540	1.00[ASN][1000 genomes]
rs12159314	1.00[ASN][1000 genomes]
rs16984270	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16984280	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16984284	1.00[ASN][1000 genomes]
rs28546189	1.00[ASN][1000 genomes]
rs480029	1.00[ASN][1000 genomes]
rs577795	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73153970	1.00[ASN][1000 genomes]
rs742054	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9613417	1.00[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	esv3413125	chr22:27404463-28121577	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
2	nsv459860	chr22:27527005-28181436	Strong transcription Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv588872	chr22:27527005-28181436	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv834166	chr22:27628570-27814359	Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs566827	VPS29	trans	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:27715200-27727400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr22:27718200-27722000	Enhancers	Fetal Brain Male	brain
3	chr22:27718600-27720200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr22:27719000-27721400	Enhancers	Fetal Brain Female	brain
5	chr22:27719200-27720200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr22:27719200-27720200	Bivalent Enhancer	Fetal Lung	lung
7	chr22:27719200-27720400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr22:27719600-27720200	Enhancers	Ovary	ovary
9	chr22:27719600-27720400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
10	chr22:27719800-27720200	Bivalent Enhancer	Fetal Stomach	stomach
11	chr22:27720000-27720200	Bivalent Enhancer	Esophagus	oesophagus
12	chr22:27720000-27725400	Weak transcription	Brain Germinal Matrix	brain

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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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