Variant report

Variant rs144619129
Chromosome Location chr11:71352169-71352170
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:71350800-71354400 Weak transcription Esophagus oesophagus
2 chr11:71351200-71353400 Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr11:71351800-71352200 Flanking Active TSS H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr11:71352000-71352200 Flanking Bivalent TSS/Enh HUES6 Cell Line embryonic stem cell
5 chr11:71352000-71352200 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
6 chr11:71352000-71352200 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
7 chr11:71352000-71357600 Weak transcription Fetal Intestine Large intestine
8 chr11:71352000-71357800 Weak transcription Fetal Intestine Small intestine

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