Variant report

Variant rs189438820
Chromosome Location chr8:11504447-11504448
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:11502200-11504600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
2 chr8:11502400-11509000 Weak transcription Gastric stomach
3 chr8:11502400-11515400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr8:11502800-11505000 Weak transcription Primary B cells from peripheral blood blood
5 chr8:11503400-11504600 Enhancers Fetal Intestine Large intestine
6 chr8:11503600-11504600 Bivalent Enhancer Fetal Intestine Small intestine
7 chr8:11503600-11509400 Weak transcription Right Atrium heart
8 chr8:11504000-11504600 Genic enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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