Variant report

Variant rs73557170
Chromosome Location chr19:41465475-41465476
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:5 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:41464800-41466400 Weak transcription Fetal Intestine Small intestine
2 chr19:41465200-41466600 Enhancers Esophagus oesophagus
3 chr19:41465400-41465800 Bivalent/Poised TSS ES-UCSF4 Cell Line embryonic stem cell
4 chr19:41465400-41465800 Active TSS Breast Myoepithelial Primary Cells Breast
5 chr19:41465400-41466000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived

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