| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110307085-110307352 | Common:3; Rare:102; Clinvar:1; Clinvar (benign):4 | ||||
| chr13:110561650-110561980 | Common:6; Rare:103 | ||||
| chr13:110615358-110615685 | Common:3; Rare:113 | ||||
| chr13:110616114-110616183 | Common:1; Rare:18 | ||||
| chr13:110705986-110706333 | Common:3; Rare:119; Clinvar:4; Clinvar (benign):8 | ||||
| chr13:110706373-110706488 | Rare:33 | ||||
| chr13:110712077-110712269 | Common:1; Rare:49 | ||||
| chr13:110712334-110713322 | Common:5; Rare:445 | ||||
| chr13:110713414-110713793 | Common:2; Rare:128 | ||||
| chr13:110714532-110714639 | Rare:38 | ||||
| chr13:110714894-110715038 | Common:1; Rare:42 | ||||
| chr13:110715183-110715930 | Common:4; Rare:350 | ||||
| chr13:110914258-110914820 | Common:8; Rare:229 | ||||
| chr13:110914893-110915621 | Common:17; Rare:265 | ||||
| chr13:111153349-111153393 | Rare:15 |