Variant report
Variant | rs28370745 |
---|---|
Chromosome Location | chr12:40383241-40383242 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:40364400-40391400 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
2 | chr12:40366400-40390200 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
3 | chr12:40380800-40384200 | Weak transcription | Colon Smooth Muscle | Colon |
4 | chr12:40380800-40393400 | Weak transcription | Rectal Mucosa Donor 29 | rectum |
5 | chr12:40382600-40383800 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
6 | chr12:40382800-40383400 | Enhancers | H1 Cell Line | embryonic stem cell |
7 | chr12:40383000-40383600 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
8 | chr12:40383200-40384400 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
9 | chr12:40383200-40384400 | Enhancers | Primary monocytes fromperipheralblood | blood |
10 | chr12:40383200-40385800 | Weak transcription | Fetal Brain Male | brain |