Variant report

Variant	rs7853385
Chromosome Location	chr9:73149897-73149898
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10780943	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10780944	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10868850	0.81[EUR][1000 genomes]
rs10868853	0.91[EUR][1000 genomes]
rs13296513	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1414850	0.93[EUR][1000 genomes]
rs17535865	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1932701	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34574970	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35112486	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57966195	0.94[EUR][1000 genomes]
rs7020777	0.93[EUR][1000 genomes]
rs7033976	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7034027	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7046672	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.87[ASN][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	nsv428219	chr9:73006269-73192535	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
2	nsv831616	chr9:73077855-73220928	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:73145400-73151000	Weak transcription	Adipose Nuclei	Adipose
2	chr9:73145400-73154000	Weak transcription	Left Ventricle	heart
3	chr9:73146800-73154000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr9:73148400-73150400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr9:73148400-73151400	Enhancers	Osteobl	bone
6	chr9:73148800-73150000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr9:73148800-73151000	Enhancers	Fetal Heart	heart
8	chr9:73149000-73150000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr9:73149200-73153800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr9:73149200-73153800	Weak transcription	Brain Angular Gyrus	brain
11	chr9:73149200-73154200	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr9:73149200-73156000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr9:73149200-73162200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr9:73149600-73150200	Enhancers	HUVEC	blood vessel
15	chr9:73149800-73150000	Enhancers	Aorta	Aorta
16	chr9:73149800-73150600	Enhancers	NHLF	lung
17	chr9:73149800-73151200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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