| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:55408058-55408119 | Rare:16 | ||||
| chr15:55408237-55408531 | Common:3; Rare:70 | ||||
| chr15:55993516-55993925 | Common:2; Rare:131 | ||||
| chr15:56918262-56918842 | Common:4; Rare:211 | ||||
| chr15:58749482-58749845 | Common:2; Rare:121 | ||||
| chr15:58770981-58771327 | Common:3; Rare:136 | ||||
| chr15:58934117-58934195 | Rare:18 | ||||
| chr15:59104904-59105218 | Common:1; Rare:106 | ||||
| chr15:59372803-59373025 | Common:1; Rare:71 | ||||
| chr15:60479081-60479171 | Common:1; Rare:33 | ||||
| chr15:62060354-62060526 | Rare:65 | ||||
| chr15:62390462-62390566 | Rare:46 | ||||
| chr15:63042609-63043124 | Rare:146; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr15:63121690-63121874 | Rare:52 | ||||
| chr15:63157099-63157244 | Rare:26 |