Variant report

Variant rs58416742
Chromosome Location chr1:77532580-77532581
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:77506000-77558600 Weak transcription Stomach Smooth Muscle stomach
2 chr1:77508600-77547600 Weak transcription Ovary ovary
3 chr1:77518200-77533400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr1:77520400-77549800 Weak transcription Fetal Stomach stomach
5 chr1:77526200-77538000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
6 chr1:77526400-77533400 Weak transcription NHEK skin
7 chr1:77526600-77533200 Weak transcription HUES64 Cell Line embryonic stem cell
8 chr1:77527200-77533800 Weak transcription Brain Anterior Caudate brain
9 chr1:77528400-77533400 Weak transcription HMEC breast
10 chr1:77529200-77549800 Weak transcription Aorta Aorta
11 chr1:77529600-77532800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr1:77530200-77537800 Strong transcription Cortex derived primary cultured neurospheres brain
13 chr1:77530600-77537000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
14 chr1:77530800-77532800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr1:77531200-77534600 Strong transcription Ganglion Eminence derived primary cultured neurospheres brain
16 chr1:77531600-77533400 Enhancers Pancreatic Islets Pancreatic Islet
17 chr1:77531600-77534400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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