| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:179559484-179559805 | Common:1; Rare:101 | ||||
| chr5:179698644-179699000 | Common:3; Rare:118 | ||||
| chr5:179820773-179820909 | Common:2; Rare:50; Clinvar (benign):1 | ||||
| chr5:179858798-179858928 | Rare:73 | ||||
| chr5:180861370-180861630 | Common:3; Rare:68 | ||||
| chr5:181223575-181223733 | Common:2; Rare:36 | ||||
| chr5:181261086-181261213 | Rare:37 | ||||
| chr6:2841844-2841868 | Rare:5 | ||||
| chr6:2841949-2842082 | Common:2; Rare:26 | ||||
| chr6:2971551-2971661 | Common:1; Rare:28 | ||||
| chr6:2999650-2999913 | Common:10; Rare:54 | ||||
| chr6:3118572-3118737 | Common:2; Rare:52 | ||||
| chr6:4021224-4021423 | Rare:93 | ||||
| chr6:5004007-5004126 | Common:1; Rare:53 | ||||
| chr6:5260873-5261048 | Common:3; Rare:70 |