Variant report

Variant rs397827382
Chromosome Location chr14:104910147-104910148
allele -/C
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104904000-104912600 Weak transcription Gastric stomach
2 chr14:104908200-104910600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
3 chr14:104908400-104910600 Bivalent Enhancer Fetal Muscle Trunk muscle
4 chr14:104908600-104910200 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr14:104908800-104910600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr14:104909000-104910600 Enhancers H1 Cell Line embryonic stem cell
7 chr14:104909400-104910200 Enhancers ES-WA7 Cell Line embryonic stem cell
8 chr14:104909400-104910200 Enhancers HUES6 Cell Line embryonic stem cell
9 chr14:104909800-104910200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
10 chr14:104910000-104912400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived

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