Variant report

Variant rs73342849
Chromosome Location chr5:177707885-177707886
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:177703600-177728800 Weak transcription Right Atrium heart
2 chr5:177706200-177708000 Bivalent Enhancer Fetal Muscle Trunk muscle
3 chr5:177706800-177708000 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin02 Skin
4 chr5:177706800-177708200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
5 chr5:177706800-177708200 Enhancers Fetal Lung lung
6 chr5:177706800-177708400 Enhancers Fetal Heart heart
7 chr5:177706800-177708600 Bivalent Enhancer Fetal Stomach stomach
8 chr5:177707200-177708000 Enhancers Placenta Placenta
9 chr5:177707200-177708400 Enhancers NHDF-Ad bronchial
10 chr5:177707400-177708000 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
11 chr5:177707400-177709600 Weak transcription Fetal Thymus thymus
12 chr5:177707400-177710600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr5:177707800-177715200 Weak transcription Cortex derived primary cultured neurospheres brain

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