Variant report

Variant rs74090518
Chromosome Location chr1:77419513-77419514
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:77393400-77429000 Weak transcription Aorta Aorta
2 chr1:77405400-77427000 Weak transcription Fetal Stomach stomach
3 chr1:77410200-77421200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr1:77411800-77421000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
5 chr1:77412200-77421400 Weak transcription HUES48 Cell Line embryonic stem cell
6 chr1:77412200-77427000 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr1:77415800-77420000 Weak transcription Cortex derived primary cultured neurospheres brain
8 chr1:77416400-77421800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr1:77416400-77427000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:77417000-77421200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr1:77417000-77425200 Weak transcription Osteobl bone
12 chr1:77417200-77421800 Weak transcription NHDF-Ad bronchial
13 chr1:77417200-77422200 Weak transcription Ovary ovary
14 chr1:77417800-77420600 Weak transcription Pancreatic Islets Pancreatic Islet

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