Variant report

Variant	rs374606616
Chromosome Location	chr21:39977997-39977998
allele	-/GAGA
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	esv3416129	chr21:39977978-39978230	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:39973000-39982000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr21:39976600-39978000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr21:39977200-39978000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr21:39977600-39982200	Weak transcription	Aorta	Aorta

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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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