| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:12129456-12129733 | Rare:111 | ||||
| chr10:12195790-12195984 | Rare:50 | ||||
| chr10:12349739-12349826 | Common:1; Rare:35 | ||||
| chr10:13099941-13100209 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):4 | ||||
| chr10:13161291-13161605 | Common:1; Rare:86 | ||||
| chr10:13300055-13300130 | Rare:28; Clinvar:1 | ||||
| chr10:13302320-13302615 | Rare:62 | ||||
| chr10:13348005-13348450 | Rare:143 | ||||
| chr10:13586794-13587031 | Common:3; Rare:77 | ||||
| chr10:14008467-14008645 | Common:1; Rare:43 | ||||
| chr10:14837915-14838386 | Common:2; Rare:147 | ||||
| chr10:14878576-14878901 | Common:2; Rare:102 | ||||
| chr10:14954023-14954304 | Common:1; Rare:93 | ||||
| chr10:14959592-14959708 | Rare:31 | ||||
| chr10:14959738-14960064 | Common:2; Rare:82 |