| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:33205948-33206132 | Rare:52 | ||||
| chr13:33285535-33285988 | Common:5; Rare:251 | ||||
| chr13:33349940-33350550 | Common:7; Rare:357 | ||||
| chr13:33350553-33350804 | Rare:177 | ||||
| chr13:33817893-33818419 | Common:5; Rare:419 | ||||
| chr13:34941796-34942145 | Rare:71 | ||||
| chr13:34942147-34942396 | Common:9; Rare:197 | ||||
| chr13:36131275-36131535 | Rare:101 | ||||
| chr13:36297121-36297513 | Common:7; Rare:124 | ||||
| chr13:36297660-36298120 | Common:6; Rare:210 | ||||
| chr13:36346221-36346604 | Common:6; Rare:185; Clinvar:6; Clinvar (benign):6 | ||||
| chr13:36346637-36347000 | Common:8; Rare:135 | ||||
| chr13:36432188-36432520 | Common:6; Rare:254 | ||||
| chr13:36819093-36819322 | Rare:86; Clinvar:3 | ||||
| chr13:36919653-36920150 | Common:9; Rare:263 |