Variant report

Variant	rs148431079
Chromosome Location	chr9:73500877-73500878
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

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	nsv893441	chr9:73486034-73594114	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv818705	chr9:73500857-73510880	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:73498400-73503600	Weak transcription	HUVEC	blood vessel
2	chr9:73499600-73501200	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr9:73500600-73501000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr9:73500600-73501800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr9:73500600-73501800	Weak transcription	NHDF-Ad	bronchial

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

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