The 2.0 version of rSNPBase

Variant report

Variant esv1782768
Chromosome Location chr4:100509973-100509975
allele n/a
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:100506200-100516000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
2 chr4:100506800-100510800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr4:100507800-100510400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
4 chr4:100507800-100533800 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr4:100508800-100510400 Weak transcription Liver Liver
6 chr4:100508800-100514000 Strong transcription HepG2 liver
7 chr4:100509000-100511400 Weak transcription Duodenum Mucosa Duodenum
8 chr4:100509000-100516000 Weak transcription Aorta Aorta
9 chr4:100509600-100510600 Genic enhancers Fetal Intestine Large intestine
10 chr4:100509800-100510200 Weak transcription Fetal Intestine Small intestine
11 chr4:100509800-100518200 Weak transcription Skeletal Muscle Female skeletal muscle

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Last update: Aug 31, 2015