Variant report

Variant rs35466827
Chromosome Location chr14:104908022-104908023
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104903000-104909000 Weak transcription H9 Cell Line embryonic stem cell
2 chr14:104903200-104909800 Weak transcription Small Intestine intestine
3 chr14:104904000-104908600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr14:104904000-104909400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
5 chr14:104904000-104912600 Weak transcription Gastric stomach
6 chr14:104904200-104909000 Weak transcription H1 Cell Line embryonic stem cell
7 chr14:104904200-104909400 Weak transcription HUES6 Cell Line embryonic stem cell
8 chr14:104904600-104908200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
9 chr14:104907800-104908200 Enhancers Fetal Brain Female brain
10 chr14:104907800-104908600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr14:104907800-104909000 Enhancers Fetal Brain Male brain
12 chr14:104907800-104910000 Enhancers Brain Germinal Matrix brain

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