| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:39688021-39688094 | Rare:23 | ||||
| chr17:39730246-39730570 | Common:1; Rare:108 | ||||
| chr17:39737775-39738000 | Rare:36 | ||||
| chr17:39738218-39738364 | Rare:35 | ||||
| chr17:39927482-39927745 | Common:2; Rare:78 | ||||
| chr17:39962814-39963040 | Common:2; Rare:48 | ||||
| chr17:40100537-40100882 | Common:2; Rare:68 | ||||
| chr17:40121838-40121989 | Common:2; Rare:59 | ||||
| chr17:40140145-40140508 | Common:5; Rare:166 | ||||
| chr17:40140690-40140779 | Rare:39 | ||||
| chr17:40181386-40181697 | Common:1; Rare:58 | ||||
| chr17:40219208-40219454 | Common:3; Rare:93 | ||||
| chr17:40342038-40342164 | Common:1; Rare:23 | ||||
| chr17:40501519-40501740 | Common:1; Rare:45 | ||||
| chr17:40819562-40820181 | Common:3; Rare:145; Clinvar (pathogenic):2 |