| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:56960731-56960998 | Rare:108 | ||||
| chr17:56961000-56961117 | Common:1; Rare:46 | ||||
| chr17:56978014-56978168 | Common:3; Rare:79 | ||||
| chr17:57084971-57085118 | Rare:52 | ||||
| chr17:57085931-57086072 | Common:1; Rare:33 | ||||
| chr17:57096401-57096638 | Rare:42 | ||||
| chr17:57256970-57257050 | Rare:32 | ||||
| chr17:57745259-57745470 | Rare:48 | ||||
| chr17:57849965-57850292 | Common:1; Rare:114 | ||||
| chr17:57988107-57988547 | Common:6; Rare:128 | ||||
| chr17:58006497-58006694 | Common:1; Rare:65 | ||||
| chr17:58007103-58007390 | Common:1; Rare:127 | ||||
| chr17:58007625-58007740 | Rare:29 | ||||
| chr17:58083187-58083546 | Common:6; Rare:138 | ||||
| chr17:58219185-58219381 | Common:1; Rare:80; Clinvar:5; Clinvar (benign):5 |