Variant report

Variant rs539078779
Chromosome Location chr7:100966607-100966608
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:100965800-100967000 Weak transcription Fetal Intestine Large intestine
2 chr7:100965800-100967200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr7:100965800-100967400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr7:100965800-100973200 Weak transcription Right Atrium heart
5 chr7:100966200-100969800 Weak transcription Fetal Muscle Leg muscle
6 chr7:100966600-100967400 Flanking Active TSS HepG2 liver

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