Variant report

Variant rs11902355
Chromosome Location chr2:179924574-179924575
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:179922200-179924600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
2 chr2:179922400-179924600 Enhancers Fetal Heart heart
3 chr2:179922600-179924800 Enhancers iPS-15b Cell Line embryonic stem cell
4 chr2:179922800-179924600 Enhancers iPS-20b Cell Line embryonic stem cell
5 chr2:179922800-179924800 Enhancers HUES48 Cell Line embryonic stem cell
6 chr2:179922800-179925200 Enhancers HUES64 Cell Line embryonic stem cell
7 chr2:179923200-179924600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr2:179923200-179924600 Enhancers HSMMtube muscle
9 chr2:179923200-179924800 Enhancers Primary B cells from cord blood blood
10 chr2:179923400-179924800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr2:179923600-179924600 Weak transcription H1 Cell Line embryonic stem cell
12 chr2:179923600-179933800 Weak transcription Gastric stomach

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