Variant report

Variant rs10514643
Chromosome Location chr2:210378048-210378049
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210363600-210378400 Weak transcription Brain Germinal Matrix brain
2 chr2:210364600-210387600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr2:210364600-210392200 Weak transcription Pancreas Pancrea
4 chr2:210366600-210387800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr2:210371400-210391000 Weak transcription Aorta Aorta
6 chr2:210372800-210381000 Strong transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr2:210373000-210380000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
8 chr2:210377400-210378200 Enhancers Primary monocytes fromperipheralblood blood
9 chr2:210377400-210378200 Enhancers Primary B cells from peripheral blood blood
10 chr2:210377400-210378800 Enhancers Fetal Brain Male brain
11 chr2:210377400-210378800 Enhancers Fetal Brain Female brain
12 chr2:210377600-210378200 Enhancers Primary B cells from cord blood blood
13 chr2:210377600-210378200 Enhancers Monocytes-CD14+_RO01746 blood
14 chr2:210377600-210378800 Flanking Active TSS Pancreatic Islets Pancreatic Islet
15 chr2:210378000-210378200 Enhancers Right Atrium heart
16 chr2:210378000-210380200 Weak transcription Cortex derived primary cultured neurospheres brain
17 chr2:210378000-210384000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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