Variant report

Variant rs72681364
Chromosome Location chr8:104914163-104914164
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:104897200-104914200 Weak transcription HUES48 Cell Line embryonic stem cell
2 chr8:104898200-104919000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr8:104899400-104933400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr8:104913200-104914600 Enhancers Fetal Intestine Large intestine
5 chr8:104913200-104914600 Enhancers Fetal Intestine Small intestine
6 chr8:104913400-104914400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr8:104914000-104914600 Enhancers HUES6 Cell Line embryonic stem cell
8 chr8:104914000-104915000 Enhancers NHDF-Ad bronchial
9 chr8:104914000-104915200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr8:104914000-104915600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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