| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47819836-47820090 | Common:2; Rare:111 | ||||
| chr12:47820380-47820822 | Common:1; Rare:117 | ||||
| chr12:47963440-47963689 | Common:4; Rare:124 | ||||
| chr12:48105060-48105403 | Common:4; Rare:97 | ||||
| chr12:48105410-48106155 | Common:7; Rare:337 | ||||
| chr12:48119148-48119408 | Common:4; Rare:102; Clinvar:8; Clinvar (benign):4 | ||||
| chr12:48157105-48158050 | Common:11; Rare:351 | ||||
| chr12:48350090-48350680 | Common:4; Rare:176 | ||||
| chr12:48350743-48351124 | Common:11; Rare:249 | ||||
| chr12:48351170-48351580 | Common:4; Rare:166 | ||||
| chr12:48682181-48682452 | Common:11; Rare:153 | ||||
| chr12:48716639-48717017 | Common:8; Rare:216 | ||||
| chr12:48788989-48789132 | Rare:69 | ||||
| chr12:48789400-48789720 | Common:4; Rare:56 | ||||
| chr12:48814683-48814927 | Rare:71 |