| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:87094602-87095340 | Common:3; Rare:353; Clinvar:7; Clinvar (benign):1 | ||||
| chr10:87504762-87504952 | Common:3; Rare:170 | ||||
| chr10:87818055-87818324 | Rare:152 | ||||
| chr10:87863269-87863711 | Common:4; Rare:285; Clinvar:171; Clinvar (benign):18 | ||||
| chr10:88991144-88991442 | Common:7; Rare:118 | ||||
| chr10:89327670-89328007 | Common:3; Rare:76 | ||||
| chr10:89392472-89392658 | Common:4; Rare:67 | ||||
| chr10:89414658-89414785 | Common:5; Rare:108 | ||||
| chr10:89643795-89644193 | Rare:160 | ||||
| chr10:89644908-89645327 | Common:10; Rare:333 | ||||
| chr10:89701330-89701666 | Common:6; Rare:213 | ||||
| chr10:91162781-91163109 | Common:2; Rare:152 | ||||
| chr10:91220016-91220303 | Rare:72 | ||||
| chr10:91410070-91410540 | Common:9; Rare:246 | ||||
| chr10:91798285-91798584 | Common:2; Rare:218 |