Variant report

Variant rs11849005
Chromosome Location chr14:81927365-81927366
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:81917000-81931000 Weak transcription Placenta Placenta
2 chr14:81919600-81927400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr14:81919600-81931000 Weak transcription Primary T regulatory cells fromperipheralblood blood
4 chr14:81921400-81930600 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr14:81926000-81931000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr14:81926200-81930800 Weak transcription Adipose Nuclei Adipose
7 chr14:81926200-81930800 Weak transcription Brain Anterior Caudate brain
8 chr14:81926200-81930800 Weak transcription Brain Germinal Matrix brain
9 chr14:81926200-81930800 Weak transcription Fetal Muscle Leg muscle
10 chr14:81926200-81930800 Weak transcription Skeletal Muscle Male skeletal muscle
11 chr14:81926200-81931000 Weak transcription Liver Liver
12 chr14:81926200-81942400 Weak transcription Spleen Spleen
13 chr14:81926400-81931000 Weak transcription Fetal Kidney kidney
14 chr14:81927200-81927400 Enhancers HepG2 liver

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