Variant report

Variant rs16884473
Chromosome Location chr4:31151060-31151061
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:31143000-31151800 Weak transcription Duodenum Smooth Muscle Duodenum
2 chr4:31145600-31154400 Weak transcription Fetal Heart heart
3 chr4:31149200-31151800 Enhancers HUES64 Cell Line embryonic stem cell
4 chr4:31149400-31151400 Enhancers iPS-15b Cell Line embryonic stem cell
5 chr4:31149600-31151600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
6 chr4:31150000-31151600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr4:31150200-31151200 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr4:31150400-31151200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr4:31150400-31151200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr4:31150400-31151200 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
11 chr4:31150400-31151200 Enhancers Fetal Lung lung
12 chr4:31150400-31151400 Enhancers HUES6 Cell Line embryonic stem cell
13 chr4:31150600-31151200 Enhancers Cortex derived primary cultured neurospheres brain
14 chr4:31150800-31151200 Enhancers iPS-20b Cell Line embryonic stem cell
15 chr4:31150800-31151200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
16 chr4:31151000-31151800 Enhancers HUES48 Cell Line embryonic stem cell

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