Variant report

Variant rs147191046
Chromosome Location chr5:177720248-177720249
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:177703600-177728800 Weak transcription Right Atrium heart
2 chr5:177718600-177720400 Weak transcription Cortex derived primary cultured neurospheres brain
3 chr5:177719000-177720800 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr5:177719000-177721000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
5 chr5:177720000-177720600 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr5:177720000-177720600 Bivalent Enhancer Fetal Muscle Trunk muscle
7 chr5:177720000-177720600 Bivalent Enhancer Fetal Muscle Leg muscle
8 chr5:177720000-177720600 Bivalent Enhancer Fetal Stomach stomach
9 chr5:177720200-177720400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr5:177720200-177720600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr5:177720200-177720800 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin

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