Variant report

Variant rs187007168
Chromosome Location chr19:51777229-51777230
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:51770400-51777400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
2 chr19:51774600-51785200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr19:51776000-51777600 Enhancers Monocytes-CD14+_RO01746 blood
4 chr19:51776000-51781000 Weak transcription K562 blood
5 chr19:51776800-51778000 Enhancers Fetal Adrenal Gland Adrenal Gland
6 chr19:51777200-51777400 Enhancers H9 Cell Line embryonic stem cell
7 chr19:51777200-51777400 Bivalent Enhancer HepG2 liver
8 chr19:51777200-51777800 Flanking Active TSS A549 lung
9 chr19:51777200-51778000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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