Variant report

Variant rs55726655
Chromosome Location chr8:104939347-104939348
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:104929400-104949600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
2 chr8:104930000-104949400 Weak transcription HUES48 Cell Line embryonic stem cell
3 chr8:104933600-104943800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr8:104938000-104949800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr8:104938400-104939400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr8:104938400-104939400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr8:104938600-104939400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr8:104938600-104939400 Enhancers Adipose Nuclei Adipose
9 chr8:104938600-104939400 Enhancers Pancreatic Islets Pancreatic Islet
10 chr8:104938800-104939400 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr8:104939000-104939400 Enhancers NHDF-Ad bronchial
12 chr8:104939000-104948600 Weak transcription HUES64 Cell Line embryonic stem cell
13 chr8:104939000-104951400 Weak transcription Fetal Adrenal Gland Adrenal Gland
14 chr8:104939000-104955200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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