Variant report

Variant	rs73626732
Chromosome Location	chr8:20447019-20447020
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs17092805	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17092806	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17092813	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17092820	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17420595	1.00[ASN][1000 genomes]
rs17420602	1.00[ASN][1000 genomes]
rs17492491	0.83[ASN][1000 genomes]
rs2410654	1.00[ASN][1000 genomes]
rs34251725	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35268784	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60455912	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7007931	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7011434	1.00[ASN][1000 genomes]
rs73626736	1.00[ASN][1000 genomes]
rs7814124	0.84[EUR][1000 genomes]
rs7816876	0.88[EUR][1000 genomes]
rs7822040	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7846105	0.82[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033511	chr8:19751299-20625091	Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv530877	chr8:19873053-20593254	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	esv2758152	chr8:20228949-20514807	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	esv2759603	chr8:20228949-20514807	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv916454	chr8:20342959-20531705	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:20445000-20455600	Weak transcription	Brain Germinal Matrix	brain
2	chr8:20446600-20448200	Enhancers	Fetal Stomach	stomach
3	chr8:20446800-20447800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr8:20446800-20448200	Enhancers	Fetal Brain Female	brain
5	chr8:20446800-20448400	Enhancers	Ovary	ovary
6	chr8:20447000-20447400	Enhancers	Fetal Lung	lung
7	chr8:20447000-20447800	Enhancers	Fetal Kidney	kidney
8	chr8:20447000-20447800	Enhancers	Fetal Muscle Leg	muscle

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