Variant report

Variant	rs59380264
Chromosome Location	chr2:21223864-21223865
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	esv3400849	chr2:21222947-21225095	Strong transcription Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21216400-21225600	Weak transcription	Aorta	Aorta
2	chr2:21220200-21225600	Weak transcription	Left Ventricle	heart
3	chr2:21220600-21224200	Weak transcription	HepG2	liver
4	chr2:21221000-21224400	Weak transcription	Fetal Intestine Small	intestine
5	chr2:21221800-21224800	Weak transcription	Fetal Intestine Large	intestine
6	chr2:21222800-21234600	Weak transcription	Adipose Nuclei	Adipose
7	chr2:21223200-21245600	Strong transcription	Liver	Liver

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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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