Variant report

Variant rs537945360
Chromosome Location chr8:11491875-11491876
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:11488600-11492200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
2 chr8:11490000-11494000 Weak transcription Fetal Intestine Large intestine
3 chr8:11490600-11492200 Weak transcription Spleen Spleen
4 chr8:11490800-11499200 Weak transcription Left Ventricle heart
5 chr8:11491000-11492000 Enhancers HepG2 liver
6 chr8:11491000-11492400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr8:11491000-11494400 Weak transcription Stomach Mucosa stomach
8 chr8:11491000-11498400 Weak transcription Pancreas Pancrea
9 chr8:11491000-11499600 Weak transcription Right Ventricle heart
10 chr8:11491200-11494200 Weak transcription Fetal Heart heart
11 chr8:11491400-11493800 Weak transcription Fetal Intestine Small intestine
12 chr8:11491400-11494400 Weak transcription Gastric stomach

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