Variant report

Variant	rs568317396
Chromosome Location	chr2:113659522-113659523
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	nsv961338	chr2:113657963-113691422	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:113655200-113659800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr2:113657400-113660600	Enhancers	Fetal Intestine Large	intestine
3	chr2:113657400-113660800	Enhancers	Fetal Intestine Small	intestine
4	chr2:113658600-113659600	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr2:113659200-113660000	Enhancers	HepG2	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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