Variant report
Variant | rs7955386 |
---|---|
Chromosome Location | chr12:29359344-29359345 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:29325400-29364600 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
2 | chr12:29346000-29360800 | Weak transcription | Duodenum Mucosa | Duodenum |
3 | chr12:29354000-29360400 | Weak transcription | Rectal Mucosa Donor 31 | rectum |
4 | chr12:29357000-29359600 | Enhancers | Primary neutrophils fromperipheralblood | blood |
5 | chr12:29357200-29359400 | Enhancers | Monocytes-CD14+_RO01746 | blood |
6 | chr12:29357400-29360200 | Enhancers | Primary monocytes fromperipheralblood | blood |
7 | chr12:29357600-29359600 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
8 | chr12:29357800-29360400 | Enhancers | Primary hematopoietic stem cells G-CSF-mobilized Female | -- |
9 | chr12:29358000-29362400 | Weak transcription | Primary T cells from cord blood | blood |
10 | chr12:29358200-29361600 | Weak transcription | Primary B cells from cord blood | blood |
11 | chr12:29358400-29362000 | Enhancers | Primary hematopoietic stem cells | blood |
12 | chr12:29359000-29359800 | Enhancers | Primary hematopoietic stem cells short term culture | blood |
13 | chr12:29359000-29360600 | Enhancers | Sigmoid Colon | Sigmoid Colon |
14 | chr12:29359200-29360200 | Weak transcription | Small Intestine | intestine |
15 | chr12:29359200-29364000 | Enhancers | Fetal Intestine Small | intestine |
16 | chr12:29359200-29366400 | Enhancers | Fetal Intestine Large | intestine |