Variant report

Variant rs73156167
Chromosome Location chr22:22835327-22835328
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:22829400-22838400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr22:22829400-22840200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr22:22829600-22839400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr22:22830600-22842800 Weak transcription Primary B cells from peripheral blood blood
5 chr22:22832600-22861800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
6 chr22:22833200-22838600 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr22:22833400-22838200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
8 chr22:22833400-22839800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
9 chr22:22833400-22854400 Weak transcription Brain Hippocampus Middle brain
10 chr22:22833600-22839000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
11 chr22:22833600-22839200 Weak transcription K562 blood
12 chr22:22834600-22836000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
13 chr22:22834800-22835400 Enhancers Fetal Intestine Small intestine
14 chr22:22834800-22835400 Flanking Active TSS HepG2 liver
15 chr22:22835200-22835600 Enhancers Liver Liver
16 chr22:22835200-22842600 Weak transcription Fetal Intestine Large intestine

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