Variant report

Variant rs672233
Chromosome Location chr13:30899601-30899602
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:30882200-30910800 Weak transcription Primary T regulatory cells fromperipheralblood blood
2 chr13:30882400-30905400 Weak transcription Right Ventricle heart
3 chr13:30882400-30905400 Weak transcription Stomach Smooth Muscle stomach
4 chr13:30886800-30900000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr13:30888000-30903400 Weak transcription Fetal Thymus thymus
6 chr13:30888000-30909600 Weak transcription Thymus Thymus
7 chr13:30889400-30906400 Weak transcription Primary B cells from cord blood blood
8 chr13:30889600-30902400 Weak transcription Primary hematopoietic stem cells blood
9 chr13:30892800-30913400 Weak transcription Psoas Muscle Psoas
10 chr13:30894200-30900200 Weak transcription Muscle Satellite Cultured Cells --
11 chr13:30894200-30903000 Weak transcription Cortex derived primary cultured neurospheres brain
12 chr13:30894800-30905400 Weak transcription Brain Anterior Caudate brain
13 chr13:30897200-30905600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr13:30898200-30903400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr13:30899600-30899800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
16 chr13:30899600-30899800 Enhancers Fetal Heart heart
17 chr13:30899600-30900000 Enhancers Dnd41 blood
18 chr13:30899600-30900400 Enhancers GM12878-XiMat blood

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