Variant report

Variant rs16932622
Chromosome Location chr11:16172069-16172070
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16168800-16172600 Enhancers Fetal Lung lung
2 chr11:16169200-16174200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr11:16169800-16174400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr11:16170400-16172600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
5 chr11:16170600-16172400 Enhancers Cortex derived primary cultured neurospheres brain
6 chr11:16170800-16172200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr11:16170800-16175800 Weak transcription Muscle Satellite Cultured Cells --
8 chr11:16171000-16173800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
9 chr11:16171000-16175200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr11:16171400-16173400 Weak transcription HepG2 liver
11 chr11:16171600-16175600 Weak transcription Fetal Intestine Large intestine
12 chr11:16171800-16172200 Weak transcription Fetal Intestine Small intestine
13 chr11:16172000-16172400 Flanking Active TSS Pancreatic Islets Pancreatic Islet
14 chr11:16172000-16173800 Weak transcription Psoas Muscle Psoas

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