Variant report

Variant rs9471052
Chromosome Location chr6:39266989-39266990
allele C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:39261400-39267400 Enhancers Fetal Adrenal Gland Adrenal Gland
2 chr6:39262600-39270600 Weak transcription Colonic Mucosa Colon
3 chr6:39263800-39267000 Enhancers Liver Liver
4 chr6:39265400-39270800 Weak transcription Fetal Lung lung
5 chr6:39265400-39270800 Weak transcription Placenta Amnion Placenta Amnion
6 chr6:39265600-39280800 Weak transcription Right Atrium heart
7 chr6:39266000-39267600 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr6:39266200-39267600 Strong transcription Breast Myoepithelial Primary Cells Breast
9 chr6:39266200-39270800 Weak transcription Monocytes-CD14+_RO01746 blood
10 chr6:39266400-39269000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr6:39266600-39270200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr6:39266600-39270400 Weak transcription Fetal Intestine Small intestine
13 chr6:39266600-39270600 Weak transcription Primary monocytes fromperipheralblood blood
14 chr6:39266600-39270600 Weak transcription Primary hematopoietic stem cells short term culture blood

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