Variant report

Variant rs138619856
Chromosome Location chr18:44547377-44547378
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:44538200-44551600 Weak transcription Gastric stomach
2 chr18:44545200-44552000 Weak transcription H1 Cell Line embryonic stem cell
3 chr18:44547000-44547400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
4 chr18:44547000-44547400 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
5 chr18:44547000-44547400 ZNF genes & repeats Fetal Stomach stomach
6 chr18:44547200-44547400 ZNF genes & repeats H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr18:44547200-44547400 ZNF genes & repeats Fetal Brain Female brain
8 chr18:44547200-44547400 Bivalent Enhancer HepG2 liver

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