Variant report

Variant rs73486997
Chromosome Location chr11:59448880-59448881
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:9 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:59446800-59449600 Enhancers Fetal Intestine Small intestine
2 chr11:59447600-59449000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr11:59447800-59450600 Enhancers Primary neutrophils fromperipheralblood blood
4 chr11:59448600-59449400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr11:59448800-59449000 Enhancers Rectal Mucosa Donor 31 rectum
6 chr11:59448800-59449200 Weak transcription Fetal Intestine Large intestine
7 chr11:59448800-59449600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr11:59448800-59450000 Enhancers K562 blood
9 chr11:59448800-59459600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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