Variant report

Variant rs114942415
Chromosome Location chr5:177720067-177720068
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:177703600-177728800 Weak transcription Right Atrium heart
2 chr5:177716600-177720200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr5:177718600-177720400 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr5:177719000-177720800 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr5:177719000-177721000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
6 chr5:177720000-177720600 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr5:177720000-177720600 Bivalent Enhancer Fetal Muscle Trunk muscle
8 chr5:177720000-177720600 Bivalent Enhancer Fetal Muscle Leg muscle
9 chr5:177720000-177720600 Bivalent Enhancer Fetal Stomach stomach

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