Variant report
Variant | rs11759157 |
---|---|
Chromosome Location | chr6:24232234-24232235 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:24214600-24235400 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
2 | chr6:24228800-24245600 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
3 | chr6:24229400-24243400 | Weak transcription | Fetal Kidney | kidney |
4 | chr6:24229800-24234600 | Strong transcription | HepG2 | liver |
5 | chr6:24230200-24242400 | Weak transcription | Pancreas | Pancrea |
6 | chr6:24230600-24234400 | Weak transcription | Primary monocytes fromperipheralblood | blood |
7 | chr6:24230600-24237200 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
8 | chr6:24231600-24232400 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
9 | chr6:24231600-24232800 | Enhancers | Colon Smooth Muscle | Colon |
10 | chr6:24231600-24232800 | Enhancers | Rectal Smooth Muscle | rectum |
11 | chr6:24232000-24263000 | Weak transcription | Fetal Intestine Small | intestine |