| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:31033574-31033911 | Common:4; Rare:82; Clinvar:6; Clinvar (benign):4 | ||||
| chr8:32548795-32548824 | Rare:14 | ||||
| chr8:33484668-33484756 | Rare:25 | ||||
| chr8:33484993-33485222 | Common:4; Rare:83 | ||||
| chr8:37736350-37736763 | Common:3; Rare:146 | ||||
| chr8:37796795-37796908 | Rare:39 | ||||
| chr8:37797323-37797490 | Common:2; Rare:35 | ||||
| chr8:37849802-37849998 | Common:1; Rare:76 | ||||
| chr8:38030085-38030714 | Common:4; Rare:174 | ||||
| chr8:38105386-38105564 | Common:3; Rare:55 | ||||
| chr8:38105728-38105995 | Rare:84 | ||||
| chr8:38176337-38176584 | Common:1; Rare:94 | ||||
| chr8:38176631-38176914 | Common:5; Rare:82 | ||||
| chr8:38231506-38231868 | Rare:96 | ||||
| chr8:38260356-38260612 | Rare:37; Clinvar (benign):1 |