Variant report

Variant rs35997966
Chromosome Location chr2:210374136-210374137
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210361800-210376400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr2:210363600-210378400 Weak transcription Brain Germinal Matrix brain
3 chr2:210364600-210387600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
4 chr2:210364600-210392200 Weak transcription Pancreas Pancrea
5 chr2:210366600-210387800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr2:210369800-210377400 Weak transcription Cortex derived primary cultured neurospheres brain
7 chr2:210371400-210391000 Weak transcription Aorta Aorta
8 chr2:210371600-210374400 Enhancers Pancreatic Islets Pancreatic Islet
9 chr2:210371800-210377400 Weak transcription Fetal Brain Female brain
10 chr2:210372800-210381000 Strong transcription H9 Derived Neuron Cultured Cells ES cell derived
11 chr2:210373000-210380000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain

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