| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:73997731-73998180 | Common:2; Rare:115 | ||||
| chr10:74150529-74150611 | Rare:20 | ||||
| chr10:74150691-74150847 | Common:2; Rare:28 | ||||
| chr10:74151029-74151305 | Common:1; Rare:80 | ||||
| chr10:74151402-74151579 | Common:1; Rare:33 | ||||
| chr10:74151696-74151782 | Rare:20 | ||||
| chr10:74175921-74176038 | Common:1; Rare:23 | ||||
| chr10:74176385-74176643 | Common:1; Rare:60 | ||||
| chr10:74176669-74176948 | Common:1; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:74824821-74825101 | Common:1; Rare:64 | ||||
| chr10:74825206-74825333 | Rare:32 | ||||
| chr10:74825694-74825940 | Rare:52 | ||||
| chr10:74825977-74826028 | Rare:10 | ||||
| chr10:74826074-74826144 | Rare:16 | ||||
| chr10:74826561-74826680 | Rare:34 |