| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:99606940-99607300 | Common:5; Rare:74 | ||||
| chr13:99971050-99971670 | Common:14; Rare:341; Clinvar:1 | ||||
| chr13:99980910-99981480 | Rare:359 | ||||
| chr13:99981485-99982190 | Common:7; Rare:666; Clinvar:2 | ||||
| chr13:99982131-99982627 | Common:1; Rare:347; Clinvar:3; Clinvar (benign):10 | ||||
| chr13:100088825-100089225 | Rare:606; Clinvar:10; Clinvar (benign):16; Clinvar (pathogenic):5 | ||||
| chr13:100588140-100589189 | Common:28; Rare:774 | ||||
| chr13:100674227-100674397 | Common:1; Rare:54 | ||||
| chr13:100674325-100675221 | Common:33; Rare:1345 | ||||
| chr13:100675141-100675541 | Common:3; Rare:135 | ||||
| chr13:102596661-102597101 | Common:6; Rare:789; Clinvar (benign):2 | ||||
| chr13:102773111-102773574 | Common:5; Rare:154 | ||||
| chr13:102773660-102774100 | Common:6; Rare:639 | ||||
| chr13:102798867-102799267 | Common:6; Rare:383 | ||||
| chr13:102799619-102800118 | Common:4; Rare:147 |