Variant report

Variant rs111203851
Chromosome Location chr12:50271716-50271717
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:50263800-50271800 Weak transcription Pancreas Pancrea
2 chr12:50266200-50275400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr12:50267000-50275800 Weak transcription Placenta Amnion Placenta Amnion
4 chr12:50267000-50297000 Weak transcription Right Atrium heart
5 chr12:50268200-50276400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr12:50269000-50274800 Strong transcription Brain Inferior Temporal Lobe brain
7 chr12:50269200-50273200 Strong transcription Brain Angular Gyrus brain
8 chr12:50269200-50274600 Weak transcription Fetal Muscle Leg muscle
9 chr12:50269400-50275400 Weak transcription Fetal Stomach stomach
10 chr12:50269800-50272000 Strong transcription Brain Hippocampus Middle brain
11 chr12:50270000-50276400 Strong transcription Brain Dorsolateral Prefrontal Cortex brain
12 chr12:50270800-50271800 Strong transcription Brain Germinal Matrix brain
13 chr12:50271200-50274600 Strong transcription Brain Cingulate Gyrus brain
14 chr12:50271400-50272200 Strong transcription Fetal Brain Female brain
15 chr12:50271400-50272200 ZNF genes & repeats K562 blood
16 chr12:50271400-50274600 Strong transcription Brain Anterior Caudate brain
17 chr12:50271600-50271800 ZNF genes & repeats Fetal Brain Male brain
18 chr12:50271600-50271800 ZNF genes & repeats Fetal Kidney kidney
19 chr12:50271600-50274800 Strong transcription Brain Substantia Nigra brain

Quick Search:


  
Input of quick search could be:

what's new

Quick links