| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:41060889-41061281 | Common:17; Rare:176 | ||||
| chr13:41061352-41061586 | Common:2; Rare:69 | ||||
| chr13:41132759-41132997 | Rare:61 | ||||
| chr13:41457315-41457551 | Common:2; Rare:68 | ||||
| chr13:43879464-43879676 | Common:1; Rare:54 | ||||
| chr13:43879691-43879910 | Common:18; Rare:62 | ||||
| chr13:44436769-44437048 | Common:2; Rare:88 | ||||
| chr13:44989419-44989653 | Rare:97 | ||||
| chr13:45120392-45120631 | Common:1; Rare:79 | ||||
| chr13:45341040-45341570 | Common:4; Rare:243 | ||||
| chr13:45464716-45465026 | Common:1; Rare:77 | ||||
| chr13:46052709-46052827 | Common:2; Rare:30 | ||||
| chr13:46553056-46553328 | Common:2; Rare:78 | ||||
| chr13:48001265-48001402 | Common:1; Rare:65; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:48233087-48233475 | Common:2; Rare:132 |