Variant report

Variant rs544953944
Chromosome Location chr15:30260176-30260177
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:30232600-30260400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr15:30257200-30260400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr15:30259200-30262200 Active TSS Brain Anterior Caudate brain
4 chr15:30259600-30260400 Enhancers Liver Liver
5 chr15:30259600-30262000 Active TSS Brain Angular Gyrus brain
6 chr15:30259800-30260600 Bivalent/Poised TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr15:30259800-30260600 Bivalent/Poised TSS Fetal Brain Male brain
8 chr15:30259800-30261600 Active TSS Brain Substantia Nigra brain
9 chr15:30259800-30261800 Active TSS Brain Cingulate Gyrus brain
10 chr15:30259800-30261800 Active TSS Brain Hippocampus Middle brain
11 chr15:30259800-30262000 Active TSS Brain Dorsolateral Prefrontal Cortex brain
12 chr15:30259800-30262600 Active TSS Brain Inferior Temporal Lobe brain
13 chr15:30260000-30260200 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell
14 chr15:30260000-30260200 Enhancers Cortex derived primary cultured neurospheres brain
15 chr15:30260000-30260200 Enhancers HMEC breast
16 chr15:30260000-30260400 Flanking Bivalent TSS/Enh Fetal Brain Female brain
17 chr15:30260000-30261400 Active TSS Ganglion Eminence derived primary cultured neurospheres brain

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