Variant report

Variant rs10492739
Chromosome Location chr13:39962791-39962792
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:39958800-39963800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr13:39959400-39965800 Weak transcription Fetal Adrenal Gland Adrenal Gland
3 chr13:39959600-39968800 Weak transcription Adipose Nuclei Adipose
4 chr13:39959800-39963000 Weak transcription Right Atrium heart
5 chr13:39960000-39979200 Weak transcription NHDF-Ad bronchial
6 chr13:39960600-39968800 Weak transcription Brain Anterior Caudate brain
7 chr13:39960600-39969000 Weak transcription Brain Germinal Matrix brain
8 chr13:39960800-39968000 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr13:39960800-39969000 Weak transcription Osteobl bone
10 chr13:39961200-39963000 Weak transcription Right Ventricle heart
11 chr13:39962000-39962800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
12 chr13:39962000-39963000 Weak transcription Left Ventricle heart
13 chr13:39962000-39963400 Weak transcription Ovary ovary
14 chr13:39962200-39963200 Weak transcription Aorta Aorta
15 chr13:39962200-39968800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
16 chr13:39962600-39963200 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived

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