Variant report

Variant rs8002004
Chromosome Location chr13:48871670-48871671
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:48844400-48877200 Weak transcription Aorta Aorta
2 chr13:48863000-48876400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
3 chr13:48866200-48876800 Weak transcription Pancreas Pancrea
4 chr13:48866200-48877200 Weak transcription Left Ventricle heart
5 chr13:48866600-48876600 Weak transcription Skeletal Muscle Female skeletal muscle
6 chr13:48868000-48876800 Weak transcription Stomach Mucosa stomach
7 chr13:48869800-48872200 Enhancers Fetal Thymus thymus
8 chr13:48870200-48877000 Weak transcription HSMMtube muscle
9 chr13:48870600-48871800 Enhancers Placenta Amnion Placenta Amnion
10 chr13:48870600-48872000 Enhancers Thymus Thymus
11 chr13:48871000-48877000 Weak transcription Primary hematopoietic stem cells short term culture blood
12 chr13:48871200-48871800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr13:48871200-48877000 Weak transcription Breast Myoepithelial Primary Cells Breast
14 chr13:48871400-48871800 Enhancers K562 blood
15 chr13:48871400-48877000 Weak transcription Primary B cells from cord blood blood
16 chr13:48871600-48872000 Flanking Active TSS Dnd41 blood
17 chr13:48871600-48876600 Weak transcription Brain Substantia Nigra brain
18 chr13:48871600-48876800 Weak transcription HepG2 liver

Quick Search:


  
Input of quick search could be:

what's new

Quick links