| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48037904-48038072 | Common:8; Rare:102 | ||||
| chr13:48095047-48095223 | Common:1; Rare:80 | ||||
| chr13:48232561-48232961 | Common:7; Rare:118 | ||||
| chr13:48233052-48233467 | Common:4; Rare:236 | ||||
| chr13:48303650-48303919 | Rare:164; Clinvar:6; Clinvar (pathogenic):2 | ||||
| chr13:48532548-48532960 | Common:12; Rare:268 | ||||
| chr13:48975747-48975950 | Common:2; Rare:100 | ||||
| chr13:48976340-48976830 | Common:5; Rare:205 | ||||
| chr13:49110216-49110391 | Common:2; Rare:54 | ||||
| chr13:49247807-49248003 | Rare:106 | ||||
| chr13:49443961-49444511 | Common:3; Rare:329 | ||||
| chr13:49585471-49585640 | Common:2; Rare:110 | ||||
| chr13:49691370-49691634 | Common:8; Rare:186 | ||||
| chr13:49792484-49792774 | Common:10; Rare:214 | ||||
| chr13:49792870-49793250 | Common:8; Rare:215 |