Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:2603229-2603466 | Common:2; Rare:108 | ||||
chr16:51152313-51152545 | Common:1; Rare:97 | ||||
chr16:72664962-72665191 | Rare:77 | ||||
chr16:74368127-74368367 | Common:1; Rare:69 | ||||
chr16:81946292-81946488 | Common:1; Rare:59 | ||||
chr16:86196125-86196149 | Rare:5 | ||||
chr16:86196184-86196343 | Common:1; Rare:49 | ||||
chr16:88100829-88100952 | Common:1; Rare:27 | ||||
chr17:7885908-7886193 | Common:4; Rare:58 | ||||
chr17:20920925-20921077 | Common:1; Rare:32 | ||||
chr17:38452394-38452453 | Common:1; Rare:8 | ||||
chr17:43315658-43315916 | Common:6; Rare:108 | ||||
chr17:47492466-47492754 | Common:2; Rare:94 | ||||
chr17:49637111-49637399 | Common:1; Rare:40 | ||||
chr17:50189419-50189684 | Rare:62; Clinvar:3; Clinvar (benign):2 |