| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:100928851-100929852 | Common:15; Rare:303 | ||||
| chr15:101008358-101008721 | Rare:197 | ||||
| chr15:101168164-101168389 | Rare:33 | ||||
| chr15:101250790-101251404 | Common:9; Rare:264; Clinvar:1; Clinvar (benign):2 | ||||
| chr15:101439621-101439801 | Common:2; Rare:28 | ||||
| chr15:101440942-101441240 | Common:3; Rare:46 | ||||
| chr15:101463347-101463533 | Common:5; Rare:36 | ||||
| chr15:101545796-101546196 | Common:10; Rare:115 | ||||
| chr15:101613593-101613802 | Common:2; Rare:45 | ||||
| chr15:101614080-101614570 | Common:5; Rare:94 | ||||
| chr15:101653132-101653390 | Common:3; Rare:94 | ||||
| chr16:10380-10700 | Common:2; Rare:51 | ||||
| chr16:12941-13354 | Common:7; Rare:43 | ||||
| chr16:71498-71692 | Rare:84 | ||||
| chr16:83404-83794 | Common:9; Rare:168 |