Variant report

Variant rs73296672
Chromosome Location chr20:22443540-22443541
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:22439200-22444000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr20:22439400-22448400 Enhancers Stomach Mucosa stomach
3 chr20:22440800-22445600 Enhancers Liver Liver
4 chr20:22441200-22443800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr20:22443200-22444200 Enhancers Pancreas Pancrea
6 chr20:22443200-22444200 Enhancers Stomach Smooth Muscle stomach
7 chr20:22443200-22444200 Enhancers HMEC breast
8 chr20:22443200-22444400 Flanking Active TSS A549 lung
9 chr20:22443200-22444600 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr20:22443200-22444600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
11 chr20:22443200-22445400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr20:22443400-22444000 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
13 chr20:22443400-22445400 Enhancers Adipose Nuclei Adipose
14 chr20:22443400-22445600 Weak transcription Gastric stomach

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