Variant report

Variant rs8048860
Chromosome Location chr16:72770337-72770338
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:72767400-72773000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr16:72769600-72770600 Enhancers HepG2 liver
3 chr16:72769800-72770400 Enhancers H1 Cell Line embryonic stem cell
4 chr16:72769800-72770400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr16:72769800-72770600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr16:72769800-72770600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
7 chr16:72769800-72770600 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
8 chr16:72769800-72770600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
9 chr16:72770000-72770400 ZNF genes & repeats H9 Derived Neuron Cultured Cells ES cell derived
10 chr16:72770000-72770600 Enhancers ES-I3 Cell Line embryonic stem cell
11 chr16:72770000-72770600 Enhancers HUES6 Cell Line embryonic stem cell
12 chr16:72770000-72770600 Enhancers iPS-15b Cell Line embryonic stem cell
13 chr16:72770000-72771000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --

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