Variant report

Variant rs10147981
Chromosome Location chr14:21372739-21372740
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:21371800-21373000 Enhancers iPS-18 Cell Line embryonic stem cell
2 chr14:21371800-21375600 Enhancers Primary monocytes fromperipheralblood blood
3 chr14:21372400-21372800 Enhancers iPS-20b Cell Line embryonic stem cell
4 chr14:21372400-21373000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
5 chr14:21372400-21373000 Enhancers HUES64 Cell Line embryonic stem cell
6 chr14:21372400-21373200 Enhancers ES-I3 Cell Line embryonic stem cell
7 chr14:21372400-21373200 Enhancers HUES48 Cell Line embryonic stem cell
8 chr14:21372400-21373200 Enhancers HUES6 Cell Line embryonic stem cell
9 chr14:21372400-21373200 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr14:21372600-21373000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr14:21372600-21373000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr14:21372600-21373000 Flanking Active TSS Monocytes-CD14+_RO01746 blood
13 chr14:21372600-21374600 Enhancers Primary hematopoietic stem cells short term culture blood
14 chr14:21372600-21374800 Enhancers Primary neutrophils fromperipheralblood blood

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