Variant report

Variant rs9398842
Chromosome Location chr6:127674662-127674663
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:127666000-127679200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
2 chr6:127666000-127704000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr6:127666200-127676800 Weak transcription Right Atrium heart
4 chr6:127666200-127687000 Weak transcription HSMM muscle
5 chr6:127667600-127676200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr6:127668800-127675800 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr6:127671800-127676000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
8 chr6:127672400-127675200 Enhancers Primary monocytes fromperipheralblood blood
9 chr6:127672600-127687000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr6:127673200-127674800 Enhancers Primary neutrophils fromperipheralblood blood
11 chr6:127673200-127675200 Enhancers Primary B cells from peripheral blood blood
12 chr6:127673400-127674800 Enhancers Primary hematopoietic stem cells short term culture blood
13 chr6:127673400-127675400 Enhancers Primary B cells from cord blood blood
14 chr6:127673800-127675600 ZNF genes & repeats H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr6:127674000-127674800 Flanking Active TSS Monocytes-CD14+_RO01746 blood

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