Variant report

Variant	rs73465705
Chromosome Location	chr9:86004269-86004270
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs6559720	0.86[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046491	chr9:85861492-86063992	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85958200-86007600	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr9:85998800-86008600	Weak transcription	Pancreas	Pancrea
3	chr9:85999400-86008400	Weak transcription	Aorta	Aorta
4	chr9:86000000-86005800	Weak transcription	Fetal Muscle Leg	muscle
5	chr9:86000000-86006600	Weak transcription	Fetal Muscle Trunk	muscle
6	chr9:86000000-86020600	Weak transcription	Fetal Brain Female	brain
7	chr9:86000400-86005600	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr9:86001200-86004400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr9:86003400-86006600	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr9:86003600-86005000	Enhancers	HepG2	liver
11	chr9:86004200-86004600	Enhancers	Gastric	stomach
12	chr9:86004200-86004800	Strong transcription	Left Ventricle	heart

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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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