Variant report

Variant rs71548605
Chromosome Location chr7:38316142-38316143
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:38311200-38317000 Enhancers Primary neutrophils fromperipheralblood blood
2 chr7:38312000-38316400 Active TSS Fetal Thymus thymus
3 chr7:38313600-38316600 Active TSS Primary Natural Killer cells fromperipheralblood blood
4 chr7:38314000-38316200 Weak transcription Primary B cells from cord blood blood
5 chr7:38315400-38316200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr7:38315800-38316600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
7 chr7:38315800-38316800 Enhancers HUES64 Cell Line embryonic stem cell
8 chr7:38315800-38316800 Enhancers iPS-18 Cell Line embryonic stem cell
9 chr7:38315800-38316800 Flanking Active TSS Primary hematopoietic stem cells short term culture blood
10 chr7:38315800-38317200 Enhancers Primary monocytes fromperipheralblood blood
11 chr7:38316000-38316400 Enhancers iPS-20b Cell Line embryonic stem cell
12 chr7:38316000-38316400 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Female --
13 chr7:38316000-38316600 Flanking Active TSS Primary hematopoietic stem cells blood
14 chr7:38316000-38316800 Enhancers ES-I3 Cell Line embryonic stem cell
15 chr7:38316000-38316800 Enhancers GM12878-XiMat blood
16 chr7:38316000-38316800 Flanking Active TSS Monocytes-CD14+_RO01746 blood

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