Variant report

Variant	rs563317333
Chromosome Location	chr15:60623536-60623537
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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	esv20296	chr15:60623455-60632031	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:60621600-60627600	Weak transcription	NHDF-Ad	bronchial
2	chr15:60621800-60627600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr15:60622200-60623800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr15:60623200-60639400	Weak transcription	Fetal Heart	heart

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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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