Variant report

Variant rs13033438
Chromosome Location chr2:133473113-133473114
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:133448600-133477000 Weak transcription Fetal Stomach stomach
2 chr2:133456000-133473400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
3 chr2:133458000-133490000 Weak transcription Brain Inferior Temporal Lobe brain
4 chr2:133460000-133479400 Weak transcription Ovary ovary
5 chr2:133468800-133485200 Weak transcription Esophagus oesophagus
6 chr2:133469200-133474400 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr2:133469600-133473600 Weak transcription Brain Cingulate Gyrus brain
8 chr2:133470600-133473800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
9 chr2:133471200-133474000 Weak transcription Brain Substantia Nigra brain
10 chr2:133472800-133473400 Enhancers Pancreatic Islets Pancreatic Islet
11 chr2:133472800-133473600 Enhancers Fetal Muscle Leg muscle
12 chr2:133473000-133473200 Enhancers Brain Hippocampus Middle brain
13 chr2:133473000-133474200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr2:133473000-133474600 Enhancers Brain Germinal Matrix brain
15 chr2:133473000-133474800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain

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