Variant report

Variant rs34102522
Chromosome Location chr6:39266479-39266480
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 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 chr6:39263000-39266600 Enhancers Placenta Placenta
4 chr6:39263800-39267000 Enhancers Liver Liver
5 chr6:39265000-39266600 Enhancers Adipose Nuclei Adipose
6 chr6:39265400-39266600 Enhancers Fetal Intestine Small intestine
7 chr6:39265400-39270800 Weak transcription Fetal Lung lung
8 chr6:39265400-39270800 Weak transcription Placenta Amnion Placenta Amnion
9 chr6:39265600-39266600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
10 chr6:39265600-39266600 Enhancers Primary monocytes fromperipheralblood blood
11 chr6:39265600-39266800 Enhancers Stomach Mucosa stomach
12 chr6:39265600-39280800 Weak transcription Right Atrium heart
13 chr6:39266000-39267600 Strong transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr6:39266200-39266600 Strong transcription Primary hematopoietic stem cells short term culture blood
15 chr6:39266200-39266800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
16 chr6:39266200-39267600 Strong transcription Breast Myoepithelial Primary Cells Breast
17 chr6:39266200-39270800 Weak transcription Monocytes-CD14+_RO01746 blood
18 chr6:39266400-39266600 Bivalent Enhancer HepG2 liver
19 chr6:39266400-39269000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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