Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:30735405-30735608 | Common:2; Rare:45 | ||||
chr13:31162333-31162441 | Common:1; Rare:28 | ||||
chr13:32031142-32031352 | Common:2; Rare:54 | ||||
chr13:32031560-32031654 | Rare:19 | ||||
chr13:32031695-32031783 | Common:1; Rare:34 | ||||
chr13:32315426-32315538 | Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
chr13:32428061-32428232 | Rare:40 | ||||
chr13:32428237-32428334 | Rare:14 | ||||
chr13:32538674-32538960 | Common:1; Rare:81 | ||||
chr13:32586248-32586597 | Common:2; Rare:108 | ||||
chr13:33205970-33206124 | Rare:32 | ||||
chr13:33285608-33285861 | Common:1; Rare:61 | ||||
chr13:33350463-33350516 | Rare:12 | ||||
chr13:33818011-33818212 | Common:1; Rare:89 | ||||
chr13:34942171-34942298 | Common:3; Rare:39 |