Variant report

Variant rs28496502
Chromosome Location chr16:47885484-47885485
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:47880400-47885600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
2 chr16:47880600-47885800 Enhancers Cortex derived primary cultured neurospheres brain
3 chr16:47882800-47889200 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
4 chr16:47883000-47890600 Weak transcription Fetal Brain Female brain
5 chr16:47883200-47889800 Weak transcription Gastric stomach
6 chr16:47883400-47899600 Weak transcription H9 Cell Line embryonic stem cell
7 chr16:47883800-47893000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr16:47884600-47885600 Enhancers Brain Anterior Caudate brain
9 chr16:47884800-47885600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr16:47884800-47885800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
11 chr16:47884800-47886000 Enhancers Brain Germinal Matrix brain
12 chr16:47885000-47885600 Enhancers Brain Substantia Nigra brain
13 chr16:47885000-47885800 Enhancers Brain Angular Gyrus brain
14 chr16:47885200-47885600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr16:47885200-47885600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr16:47885400-47886600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
17 chr16:47885400-47891000 Weak transcription Fetal Brain Male brain

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