Variant report

Variant rs9461876
Chromosome Location chr6:33516657-33516658
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:33514000-33519800 Enhancers Placenta Placenta
2 chr6:33514600-33516800 Enhancers Primary T helper naive cells fromperipheralblood blood
3 chr6:33515000-33516800 Enhancers Primary T cells fromperipheralblood blood
4 chr6:33515200-33516800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
5 chr6:33515200-33517000 Enhancers Primary hematopoietic stem cells blood
6 chr6:33515400-33516800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr6:33515400-33517200 Enhancers Primary hematopoietic stem cells short term culture blood
8 chr6:33515600-33517000 Weak transcription K562 blood
9 chr6:33515800-33517200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr6:33516000-33517200 Enhancers Primary neutrophils fromperipheralblood blood
11 chr6:33516000-33523800 Weak transcription GM12878-XiMat blood
12 chr6:33516400-33517200 Enhancers HUES6 Cell Line embryonic stem cell
13 chr6:33516400-33517400 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
14 chr6:33516600-33518000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr6:33516600-33521800 Weak transcription Primary T cells from cord blood blood

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