Variant report

Variant	rs575332614
Chromosome Location	chr12:118240882-118240883
allele	G/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	esv988370	chr12:118240136-118249923	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118232600-118246400	Weak transcription	Pancreas	Pancrea
2	chr12:118237200-118254000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:118240200-118241200	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr12:118240400-118241000	Enhancers	Fetal Intestine Large	intestine
5	chr12:118240600-118241000	Enhancers	Liver	Liver
6	chr12:118240600-118241200	Enhancers	HepG2	liver
7	chr12:118240600-118241400	Enhancers	Rectal Mucosa Donor 29	rectum
8	chr12:118240600-118241600	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr12:118240600-118241800	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr12:118240800-118241600	Weak transcription	Fetal Intestine Small	intestine

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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