| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:32350021-32350204 | Rare:99 | ||||
| chr17:32927905-32928215 | Common:1; Rare:105 | ||||
| chr17:34255039-34255293 | Rare:59 | ||||
| chr17:34961489-34961579 | Common:1; Rare:45 | ||||
| chr17:34980466-34980604 | Common:4; Rare:41 | ||||
| chr17:34981146-34981179 | Rare:6 | ||||
| chr17:35242900-35243081 | Rare:60 | ||||
| chr17:35578496-35578684 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:35587016-35587478 | Common:2; Rare:119 | ||||
| chr17:36544796-36544997 | Common:3; Rare:65 | ||||
| chr17:37406812-37406935 | Rare:45 | ||||
| chr17:37489581-37489900 | Common:2; Rare:120 | ||||
| chr17:37609362-37609622 | Common:1; Rare:112 | ||||
| chr17:37643422-37643482 | Rare:26 | ||||
| chr17:38296888-38297183 | Common:5; Rare:88 |