Variant report

Variant rs16932655
Chromosome Location chr11:16183163-16183164
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16172400-16191400 Weak transcription Cortex derived primary cultured neurospheres brain
2 chr11:16172600-16191400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr11:16174200-16191200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr11:16177600-16187800 Weak transcription Fetal Intestine Small intestine
5 chr11:16178000-16185200 Weak transcription Fetal Intestine Large intestine
6 chr11:16181800-16183400 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr11:16181800-16183400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr11:16182000-16183200 Weak transcription Skeletal Muscle Female skeletal muscle
9 chr11:16182000-16191600 Weak transcription Psoas Muscle Psoas
10 chr11:16182800-16190800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr11:16183000-16183400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived

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