| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:102502016-102502377 | Common:3; Rare:110 | ||||
| chr10:102502655-102502888 | Common:1; Rare:79 | ||||
| chr10:102503769-102504141 | Common:3; Rare:104; Clinvar:3; Clinvar (benign):2 | ||||
| chr10:102644192-102644248 | Rare:15 | ||||
| chr10:102645384-102645498 | Rare:19 | ||||
| chr10:102648949-102649165 | Common:5; Rare:52 | ||||
| chr10:102713685-102713951 | Rare:59 | ||||
| chr10:102714258-102714740 | Common:3; Rare:150 | ||||
| chr10:102715000-102715070 | Common:1; Rare:12 | ||||
| chr10:102853986-102854337 | Common:2; Rare:116 | ||||
| chr10:102854399-102854663 | Common:1; Rare:73 | ||||
| chr10:102869380-102869497 | Common:1; Rare:31 | ||||
| chr10:102918425-102918630 | Common:1; Rare:75; Clinvar (benign):1 | ||||
| chr10:103193235-103193402 | Common:5; Rare:56; Clinvar (benign):1 | ||||
| chr10:103350540-103350669 | Rare:39 |