| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:100687816-100688107 | Common:3; Rare:63 | ||||
| chr15:100713448-100713714 | Common:3; Rare:53 | ||||
| chr15:100721660-100721857 | Common:2; Rare:45 | ||||
| chr15:100721961-100722163 | Rare:37 | ||||
| chr15:100849493-100849758 | Common:1; Rare:72 | ||||
| chr15:100861750-100861944 | Common:1; Rare:42 | ||||
| chr15:100911446-100911643 | Rare:28 | ||||
| chr15:100913712-100913991 | Common:3; Rare:36 | ||||
| chr16:263540-263668 | Common:1; Rare:39 | ||||
| chr16:505377-505598 | Common:1; Rare:50 | ||||
| chr16:528798-529121 | Common:2; Rare:82 | ||||
| chr16:1511050-1511320 | Common:1; Rare:111; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr16:2170182-2170368 | Rare:48 | ||||
| chr16:2603241-2603466 | Common:2; Rare:100 | ||||
| chr16:2673302-2673715 | Common:10; Rare:147 |