Variant report

Variant rs4991798
Chromosome Location chr22:22533305-22533306
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:22521600-22536800 Weak transcription Right Atrium heart
2 chr22:22531000-22534800 Weak transcription Fetal Kidney kidney
3 chr22:22532800-22533400 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
4 chr22:22532800-22533800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr22:22532800-22533800 Enhancers Primary B cells from peripheral blood blood
6 chr22:22532800-22533800 Enhancers Dnd41 blood
7 chr22:22533000-22533400 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
8 chr22:22533000-22533400 Bivalent Enhancer hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr22:22533000-22533400 Bivalent Enhancer HUES64 Cell Line embryonic stem cell
10 chr22:22533000-22533800 Enhancers Primary B cells from cord blood blood
11 chr22:22533200-22533400 Bivalent Enhancer H1 Cell Line embryonic stem cell
12 chr22:22533200-22533400 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
13 chr22:22533200-22533600 Enhancers Fetal Thymus thymus
14 chr22:22533200-22533800 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
15 chr22:22533200-22533800 Enhancers GM12878-XiMat blood
16 chr22:22533200-22536200 Active TSS Pancreatic Islets Pancreatic Islet

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