Variant report

Variant rs139427976
Chromosome Location chr6:139933415-139933416
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:139929200-139941000 Weak transcription Aorta Aorta
2 chr6:139929200-139944000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr6:139931600-139933600 Enhancers iPS-18 Cell Line embryonic stem cell
4 chr6:139932000-139933600 Enhancers HUES64 Cell Line embryonic stem cell
5 chr6:139932000-139933800 Enhancers Primary neutrophils fromperipheralblood blood
6 chr6:139932200-139933600 Enhancers iPS-20b Cell Line embryonic stem cell
7 chr6:139932200-139933600 Enhancers Primary monocytes fromperipheralblood blood
8 chr6:139932200-139935000 Enhancers Cortex derived primary cultured neurospheres brain
9 chr6:139932400-139933600 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr6:139932600-139933600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr6:139932600-139933600 Enhancers iPS-15b Cell Line embryonic stem cell
12 chr6:139932600-139933800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr6:139932800-139933600 Flanking Active TSS Monocytes-CD14+_RO01746 blood
14 chr6:139932800-139934000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
15 chr6:139933400-139938600 Weak transcription K562 blood

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