Variant report
Variant | rs7039117 |
---|---|
Chromosome Location | chr9:98057180-98057181 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:98046600-98059400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
2 | chr9:98046600-98063000 | Weak transcription | Fetal Stomach | stomach |
3 | chr9:98047200-98059400 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
4 | chr9:98048800-98059200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
5 | chr9:98050000-98059200 | Weak transcription | HSMM | muscle |
6 | chr9:98050200-98067400 | Weak transcription | A549 | lung |
7 | chr9:98051200-98059400 | Weak transcription | Small Intestine | intestine |
8 | chr9:98054600-98059400 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
9 | chr9:98054800-98063000 | Weak transcription | Lung | lung |
10 | chr9:98055000-98068600 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
11 | chr9:98055200-98065600 | Weak transcription | Thymus | Thymus |
12 | chr9:98055400-98066000 | Weak transcription | Fetal Muscle Leg | muscle |
13 | chr9:98055600-98062000 | Weak transcription | Aorta | Aorta |
14 | chr9:98056200-98059600 | Weak transcription | Fetal Intestine Small | intestine |
15 | chr9:98057000-98059000 | Weak transcription | HepG2 | liver |
16 | chr9:98057000-98059400 | Weak transcription | Fetal Intestine Large | intestine |
17 | chr9:98057000-98059400 | Weak transcription | Sigmoid Colon | Sigmoid Colon |