Variant report

Variant rs10790348
Chromosome Location chr11:119679921-119679922
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:119677800-119682400 Weak transcription Fetal Intestine Large intestine
2 chr11:119677800-119683800 Weak transcription Right Ventricle heart
3 chr11:119678200-119680800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr11:119678800-119680400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr11:119679400-119680000 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr11:119679400-119680800 Bivalent Enhancer Fetal Stomach stomach
7 chr11:119679800-119680000 Bivalent Enhancer Fetal Muscle Trunk muscle
8 chr11:119679800-119680400 Bivalent Enhancer Fetal Muscle Leg muscle
9 chr11:119679800-119681800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived

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