Variant report

Variant	rs73388519
Chromosome Location	chr12:106677048-106677049
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:106666200-106680800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr12:106674000-106677200	Enhancers	Fetal Heart	heart
3	chr12:106676000-106677200	Enhancers	Liver	Liver
4	chr12:106676200-106678200	Weak transcription	NHEK	skin
5	chr12:106676200-106679200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr12:106676400-106677200	Enhancers	Fetal Intestine Large	intestine
7	chr12:106676400-106677200	Enhancers	Fetal Intestine Small	intestine
8	chr12:106676600-106681000	Weak transcription	Stomach Mucosa	stomach
9	chr12:106676800-106677200	Flanking Active TSS	HepG2	liver
10	chr12:106677000-106681400	Weak transcription	Rectal Mucosa Donor 31	rectum

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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