Variant report

Variant rs7166003
Chromosome Location chr15:78861517-78861518
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:78859000-78868400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr15:78859200-78882400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr15:78859600-78861600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr15:78860000-78865800 Weak transcription Fetal Brain Female brain
5 chr15:78860200-78863200 Weak transcription A549 lung
6 chr15:78860200-78881400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr15:78860200-78881600 Weak transcription HUES48 Cell Line embryonic stem cell
8 chr15:78860200-78882200 Weak transcription Hela-S3 cervix
9 chr15:78860400-78864200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr15:78860600-78864200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr15:78861200-78865200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
12 chr15:78861400-78861800 Enhancers GM12878-XiMat blood

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