Variant report

Variant rs34688771
Chromosome Location chr5:177773824-177773825
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:177759400-177783400 Weak transcription Right Atrium heart
2 chr5:177762600-177775400 Weak transcription Thymus Thymus
3 chr5:177768200-177783000 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr5:177769400-177774000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr5:177769600-177783200 Weak transcription Fetal Thymus thymus
6 chr5:177772600-177774000 Weak transcription Brain Substantia Nigra brain
7 chr5:177773200-177775600 Enhancers Brain Cingulate Gyrus brain
8 chr5:177773400-177774000 Enhancers Brain Hippocampus Middle brain
9 chr5:177773400-177774200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
10 chr5:177773400-177775600 Enhancers Brain Inferior Temporal Lobe brain
11 chr5:177773800-177774000 Flanking Active TSS H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr5:177773800-177774000 Bivalent Enhancer Fetal Muscle Trunk muscle
13 chr5:177773800-177774200 Enhancers Brain Dorsolateral Prefrontal Cortex brain
14 chr5:177773800-177774200 Bivalent Enhancer Fetal Stomach stomach

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