Variant report

Variant rs73962062
Chromosome Location chr2:145427816-145427817
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:145416800-145431400 Enhancers Primary monocytes fromperipheralblood blood
2 chr2:145419000-145432800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr2:145422600-145429000 Weak transcription Primary hematopoietic stem cells short term culture blood
4 chr2:145423000-145440600 Weak transcription Primary hematopoietic stem cells blood
5 chr2:145424000-145433000 Weak transcription HMEC breast
6 chr2:145424600-145428600 Weak transcription Primary neutrophils fromperipheralblood blood
7 chr2:145426400-145428000 Flanking Active TSS Monocytes-CD14+_RO01746 blood
8 chr2:145426600-145430000 Enhancers Primary B cells from cord blood blood
9 chr2:145427200-145428000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr2:145427200-145429800 Enhancers Primary B cells from peripheral blood blood
11 chr2:145427400-145428000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr2:145427400-145428000 Enhancers Primary Natural Killer cells fromperipheralblood blood
13 chr2:145427600-145428000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived

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