Variant report

Variant rs12579406
Chromosome Location chr12:42310151-42310152
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:42300000-42311800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr12:42302200-42311600 Weak transcription Fetal Lung lung
3 chr12:42302200-42311600 Weak transcription Right Atrium heart
4 chr12:42302400-42311800 Weak transcription H9 Cell Line embryonic stem cell
5 chr12:42308400-42311600 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr12:42308400-42311600 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
7 chr12:42308600-42311600 Weak transcription Cortex derived primary cultured neurospheres brain
8 chr12:42309400-42310400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr12:42309600-42310200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr12:42309600-42310200 Enhancers Primary hematopoietic stem cells blood
11 chr12:42309600-42310200 Enhancers Brain Germinal Matrix brain
12 chr12:42309600-42310400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr12:42309600-42310400 Enhancers Fetal Adrenal Gland Adrenal Gland
14 chr12:42309600-42312600 Enhancers HUVEC blood vessel
15 chr12:42309800-42310200 Enhancers Primary hematopoietic stem cells short term culture blood
16 chr12:42309800-42311600 Weak transcription Fetal Heart heart
17 chr12:42310000-42310200 Enhancers HUES48 Cell Line embryonic stem cell

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