Variant report

Variant rs11145913
Chromosome Location chr9:139774853-139774854
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139767400-139775000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr9:139770800-139775800 Weak transcription K562 blood
3 chr9:139771200-139775200 Weak transcription Placenta Placenta
4 chr9:139771400-139775000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr9:139771400-139775800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
6 chr9:139774000-139776400 Weak transcription Right Atrium heart
7 chr9:139774800-139775200 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
8 chr9:139774800-139776000 Enhancers GM12878-XiMat blood
9 chr9:139774800-139776400 Enhancers Fetal Intestine Small intestine

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