| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:20330657-20330750 | Rare:27 | ||||
| chr7:20330922-20331071 | Common:2; Rare:36 | ||||
| chr7:20331719-20331846 | Common:1; Rare:43 | ||||
| chr7:22822709-22822954 | Common:3; Rare:92 | ||||
| chr7:23105687-23105841 | Common:2; Rare:85; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181767-23181802 | Rare:9 | ||||
| chr7:23181814-23181861 | Rare:16 | ||||
| chr7:23181864-23182135 | Common:1; Rare:115 | ||||
| chr7:23470292-23470560 | Rare:81 | ||||
| chr7:23531884-23532083 | Common:2; Rare:79 | ||||
| chr7:23680019-23680208 | Common:5; Rare:54 | ||||
| chr7:24757394-24757621 | Common:2; Rare:68 | ||||
| chr7:24980108-24980360 | Common:6; Rare:104 | ||||
| chr7:25125198-25125443 | Rare:106; Clinvar:3 | ||||
| chr7:26200573-26200941 | Common:1; Rare:180 |