Variant report

Variant rs948526
Chromosome Location chr18:29143317-29143318
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:29136600-29145400 Weak transcription Fetal Intestine Small intestine
2 chr18:29142200-29143800 Enhancers HepG2 liver
3 chr18:29142600-29143600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr18:29142600-29145600 Enhancers Liver Liver
5 chr18:29143000-29144200 Weak transcription Fetal Intestine Large intestine
6 chr18:29143200-29143400 Enhancers Pancreatic Islets Pancreatic Islet
7 chr18:29143200-29143400 Enhancers Gastric stomach

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