Variant report

Variant rs190405293
Chromosome Location chr11:16112315-16112316
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16083200-16116000 Weak transcription Fetal Intestine Large intestine
2 chr11:16089400-16117400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr11:16097000-16115600 Weak transcription Psoas Muscle Psoas
4 chr11:16098600-16137000 Weak transcription Pancreas Pancrea
5 chr11:16104600-16114400 Weak transcription Liver Liver
6 chr11:16104800-16112600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr11:16108200-16112600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr11:16108200-16113800 Weak transcription Brain Germinal Matrix brain
9 chr11:16108200-16114200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr11:16108400-16112600 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr11:16108400-16118400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
12 chr11:16108800-16112600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
13 chr11:16112000-16112800 Weak transcription Pancreatic Islets Pancreatic Islet
14 chr11:16112200-16112600 Weak transcription Cortex derived primary cultured neurospheres brain

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