Variant report

Variant rs28431469
Chromosome Location chr6:132930611-132930612
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:132926200-132933600 Weak transcription Stomach Mucosa stomach
2 chr6:132926600-132931800 Weak transcription Small Intestine intestine
3 chr6:132928000-132935200 Enhancers Fetal Intestine Small intestine
4 chr6:132928200-132932200 Enhancers Fetal Intestine Large intestine
5 chr6:132929000-132933600 Weak transcription HepG2 liver
6 chr6:132929400-132931600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr6:132929600-132932000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr6:132929800-132931800 Weak transcription Pancreas Pancrea
9 chr6:132930000-132931800 Weak transcription Liver Liver
10 chr6:132930400-132930800 Weak transcription Brain Substantia Nigra brain
11 chr6:132930400-132931400 Weak transcription Duodenum Mucosa Duodenum
12 chr6:132930400-132934000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
13 chr6:132930400-132935600 Weak transcription Cortex derived primary cultured neurospheres brain
14 chr6:132930600-132931600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr6:132930600-132932000 Enhancers Monocytes-CD14+_RO01746 blood

Quick Search:


  
Input of quick search could be:

what's new

Quick links