Variant report

Variant rs10078847
Chromosome Location chr5:59821217-59821218
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:59812800-59822400 Weak transcription Brain Angular Gyrus brain
2 chr5:59817000-59822000 Weak transcription Fetal Thymus thymus
3 chr5:59817400-59822000 Weak transcription Brain Substantia Nigra brain
4 chr5:59817800-59829000 Weak transcription Aorta Aorta
5 chr5:59818000-59822000 Weak transcription Dnd41 blood
6 chr5:59818000-59822400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr5:59818000-59822400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
8 chr5:59818400-59822600 Weak transcription Brain Hippocampus Middle brain
9 chr5:59818600-59821600 Weak transcription Primary T cells from cord blood blood
10 chr5:59819200-59822000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
11 chr5:59819600-59822000 Weak transcription Stomach Smooth Muscle stomach
12 chr5:59819600-59824800 Weak transcription Primary monocytes fromperipheralblood blood
13 chr5:59819600-59825000 Weak transcription Monocytes-CD14+_RO01746 blood
14 chr5:59820000-59825000 Weak transcription Rectal Smooth Muscle rectum
15 chr5:59820200-59822000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
16 chr5:59820200-59824600 Weak transcription Primary B cells from cord blood blood

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