Variant report

Variant rs534460779
Chromosome Location chr7:39123780-39123781
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:39115600-39125200 Weak transcription H1 Cell Line embryonic stem cell
2 chr7:39122400-39124000 Weak transcription iPS-18 Cell Line embryonic stem cell
3 chr7:39122600-39125000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
4 chr7:39122800-39125000 Weak transcription HUES6 Cell Line embryonic stem cell
5 chr7:39123000-39124400 Weak transcription ES-I3 Cell Line embryonic stem cell
6 chr7:39123200-39124400 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
7 chr7:39123200-39124800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr7:39123200-39125000 Enhancers Fetal Brain Male brain
9 chr7:39123400-39123800 Enhancers Pancreatic Islets Pancreatic Islet
10 chr7:39123400-39124400 Weak transcription HUES64 Cell Line embryonic stem cell
11 chr7:39123600-39124400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr7:39123600-39125000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived

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