Variant report

Variant rs377976
Chromosome Location chr22:22831235-22831236
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:22815800-22832800 Weak transcription Right Atrium heart
2 chr22:22829400-22832800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr22:22829400-22832800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr22:22829400-22833400 Weak transcription Fetal Intestine Large intestine
5 chr22:22829400-22834800 Weak transcription Fetal Intestine Small intestine
6 chr22:22829400-22838400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr22:22829400-22840200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
8 chr22:22829600-22834600 Weak transcription HepG2 liver
9 chr22:22829600-22839400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr22:22830600-22842800 Weak transcription Primary B cells from peripheral blood blood
11 chr22:22831000-22833400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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