| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:93227145-93227452 | Rare:76; Clinvar:6 | ||||
| chr13:94601606-94601924 | Common:3; Rare:92 | ||||
| chr13:95676930-95677200 | Common:3; Rare:95 | ||||
| chr13:96053344-96053588 | Common:2; Rare:104 | ||||
| chr13:97222154-97222406 | Rare:43 | ||||
| chr13:97975665-97975967 | Common:3; Rare:80 | ||||
| chr13:99200668-99200898 | Common:6; Rare:107 | ||||
| chr13:100088894-100089120 | Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:100674778-100675060 | Common:3; Rare:115 | ||||
| chr13:102596792-102597162 | Common:2; Rare:147; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:102773740-102773842 | Rare:51 | ||||
| chr13:102798939-102799207 | Common:1; Rare:56 | ||||
| chr13:102845707-102846124 | Common:9; Rare:112; Clinvar:3; Clinvar (benign):4 | ||||
| chr13:106568076-106568267 | Rare:59 | ||||
| chr13:108215500-108215729 | Common:1; Rare:60 |