Variant report

Variant rs559303884
Chromosome Location chr13:95618512-95618513
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:95616400-95619600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr13:95617600-95618800 Enhancers iPS-20b Cell Line embryonic stem cell
3 chr13:95617800-95618800 Enhancers HUES48 Cell Line embryonic stem cell
4 chr13:95617800-95619200 Enhancers Stomach Mucosa stomach
5 chr13:95618000-95618600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr13:95618000-95618800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
7 chr13:95618000-95619000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
8 chr13:95618000-95619400 Bivalent Enhancer HUES64 Cell Line embryonic stem cell
9 chr13:95618000-95619400 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
10 chr13:95618400-95618600 Bivalent Enhancer Fetal Brain Male brain
11 chr13:95618400-95619400 Flanking Active TSS H9 Derived Neuron Cultured Cells ES cell derived
12 chr13:95618400-95619400 Bivalent Enhancer hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr13:95618400-95619600 Enhancers Brain Germinal Matrix brain
14 chr13:95618400-95619600 Bivalent Enhancer Brain Hippocampus Middle brain

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