Variant report
Variant | rs60017659 |
---|---|
Chromosome Location | chr8:67670543-67670544 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr8:67647800-67671000 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
2 | chr8:67652200-67672400 | Weak transcription | Fetal Intestine Small | intestine |
3 | chr8:67656400-67679000 | Weak transcription | Sigmoid Colon | Sigmoid Colon |
4 | chr8:67661000-67673400 | Weak transcription | Brain Hippocampus Middle | brain |
5 | chr8:67664600-67686400 | Weak transcription | Right Atrium | heart |
6 | chr8:67664800-67670800 | Weak transcription | Brain Anterior Caudate | brain |
7 | chr8:67665000-67671600 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
8 | chr8:67665800-67673000 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
9 | chr8:67666000-67673200 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
10 | chr8:67668600-67671000 | Weak transcription | Brain Substantia Nigra | brain |
11 | chr8:67668600-67672800 | Weak transcription | Brain Inferior Temporal Lobe | brain |
12 | chr8:67668800-67670800 | Weak transcription | Brain Cingulate Gyrus | brain |
13 | chr8:67670400-67671800 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |