Variant report

Variant rs72898661
Chromosome Location chr11:45699413-45699414
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:45688000-45700600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr11:45694200-45699600 Weak transcription Brain Angular Gyrus brain
3 chr11:45699000-45700000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr11:45699000-45700000 Enhancers Fetal Heart heart
5 chr11:45699000-45700000 Bivalent Enhancer Fetal Muscle Trunk muscle
6 chr11:45699000-45700600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
7 chr11:45699200-45699600 Enhancers H1 Cell Line embryonic stem cell
8 chr11:45699200-45699600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr11:45699200-45699600 Enhancers iPS-18 Cell Line embryonic stem cell
10 chr11:45699200-45699600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
11 chr11:45699200-45699800 Enhancers Placenta Placenta
12 chr11:45699200-45700000 Enhancers ES-WA7 Cell Line embryonic stem cell
13 chr11:45699200-45700000 Enhancers Brain Germinal Matrix brain
14 chr11:45699200-45700800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
15 chr11:45699400-45699600 Enhancers ES-I3 Cell Line embryonic stem cell

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