| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:88583290-88583383 | Rare:21 | ||||
| chr10:88952731-88952969 | Rare:36; Clinvar:1 | ||||
| chr10:88990374-88990870 | Common:6; Rare:125; Clinvar:1; Clinvar (benign):5 | ||||
| chr10:88991310-88991451 | Common:2; Rare:28 | ||||
| chr10:89301869-89302079 | Rare:44 | ||||
| chr10:89332261-89332543 | Common:3; Rare:46 | ||||
| chr10:89414680-89414785 | Common:3; Rare:50 | ||||
| chr10:89701440-89701620 | Common:1; Rare:44 | ||||
| chr10:91410240-91410502 | Common:3; Rare:97 | ||||
| chr10:91633056-91633359 | Common:2; Rare:90 | ||||
| chr10:91923716-91923826 | Common:1; Rare:43 | ||||
| chr10:92291022-92291490 | Common:6; Rare:152 | ||||
| chr10:92574008-92574149 | Common:1; Rare:44 | ||||
| chr10:93482213-93482330 | Common:2; Rare:39 | ||||
| chr10:93757666-93758020 | Common:1; Rare:59; Clinvar:3; Clinvar (benign):1 |