Variant report

Variant rs56376672
Chromosome Location chr5:148147672-148147673
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:148139000-148149200 Enhancers Primary neutrophils fromperipheralblood blood
2 chr5:148145000-148149400 Enhancers Primary monocytes fromperipheralblood blood
3 chr5:148145800-148149800 Enhancers Primary hematopoietic stem cells short term culture blood
4 chr5:148146600-148148200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr5:148146600-148148400 Weak transcription HMEC breast
6 chr5:148146600-148148800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr5:148146600-148149000 Weak transcription NHEK skin
8 chr5:148146600-148153400 Weak transcription Primary B cells from cord blood blood
9 chr5:148146600-148153600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr5:148146600-148155600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr5:148146800-148148600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr5:148147200-148148400 Weak transcription Fetal Heart heart
13 chr5:148147600-148148800 Flanking Active TSS Monocytes-CD14+_RO01746 blood

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