| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:27268729-27268850 | Common:1; Rare:37 | ||||
| chr16:27549891-27550162 | Common:2; Rare:97 | ||||
| chr16:29996103-29996283 | Common:2; Rare:66 | ||||
| chr16:30355211-30355443 | Common:1; Rare:82 | ||||
| chr16:30534972-30535070 | Common:1; Rare:32 | ||||
| chr16:30893966-30894275 | Common:5; Rare:81 | ||||
| chr16:31508374-31508478 | Common:1; Rare:41 | ||||
| chr16:46689140-46689417 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:46973615-46973772 | Rare:74 | ||||
| chr16:47461052-47461362 | Common:2; Rare:109; Clinvar (benign):2 | ||||
| chr16:53703828-53704190 | Rare:106; Clinvar:4 | ||||
| chr16:56451322-56451567 | Common:1; Rare:65 | ||||
| chr16:57186001-57186342 | Common:1; Rare:102 | ||||
| chr16:57447360-57447527 | Common:2; Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
| chr16:66552451-66552661 | Rare:90 |