Variant report

Variant	rs1647255
Chromosome Location	chr12:121815262-121815263
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121814400-121815400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr12:121814400-121815400	Enhancers	Fetal Intestine Large	intestine
3	chr12:121814400-121815400	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr12:121814600-121815400	Enhancers	Fetal Intestine Small	intestine
5	chr12:121814600-121815400	Enhancers	Fetal Kidney	kidney
6	chr12:121814600-121815400	Flanking Active TSS	HepG2	liver
7	chr12:121814600-121815800	Enhancers	Pancreas	Pancrea
8	chr12:121814600-121815800	Enhancers	Stomach Mucosa	stomach
9	chr12:121815000-121815400	Enhancers	Liver	Liver
10	chr12:121815000-121815600	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr12:121815200-121815600	Enhancers	A549	lung

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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