| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34438580-34439045 | Common:3; Rare:141; Clinvar (benign):1 | ||||
| chr11:34439111-34439214 | Common:2; Rare:27 | ||||
| chr11:34915698-34915775 | Common:1; Rare:11 | ||||
| chr11:34915884-34916229 | Common:4; Rare:100; Clinvar (benign):2 | ||||
| chr11:34916236-34916733 | Common:14; Rare:199; Clinvar:8; Clinvar (benign):15; Clinvar (pathogenic):1 | ||||
| chr11:34916863-34916904 | Rare:14 | ||||
| chr11:35138711-35138906 | Common:2; Rare:43 | ||||
| chr11:35138952-35139288 | Common:1; Rare:85 | ||||
| chr11:35139339-35139456 | Rare:32 | ||||
| chr11:35139572-35139785 | Common:2; Rare:49 | ||||
| chr11:35617920-35618076 | Rare:27 | ||||
| chr11:35619487-35619845 | Common:1; Rare:128 | ||||
| chr11:35662159-35662447 | Common:1; Rare:49 | ||||
| chr11:35662584-35662934 | Common:3; Rare:110 | ||||
| chr11:35662972-35663252 | Rare:82 |