| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:27503978-27504440 | Common:1; Rare:182; Clinvar:5; Clinvar (benign):1 | ||||
| chr10:27504500-27504706 | Rare:72 | ||||
| chr10:27504720-27504751 | Rare:9 | ||||
| chr10:27743113-27743315 | Common:3; Rare:75 | ||||
| chr10:27743623-27743749 | Rare:35 | ||||
| chr10:28532107-28532513 | Common:2; Rare:115 | ||||
| chr10:28532561-28533337 | Common:5; Rare:313 | ||||
| chr10:28533354-28533407 | Rare:14 | ||||
| chr10:28533674-28533863 | Common:2; Rare:66 | ||||
| chr10:28534184-28534223 | Common:1; Rare:13 | ||||
| chr10:28677245-28677670 | Common:8; Rare:193 | ||||
| chr10:29634953-29635072 | Rare:18 | ||||
| chr10:29735244-29735358 | Common:1; Rare:27 | ||||
| chr10:29735558-29735965 | Common:7; Rare:105 | ||||
| chr10:29736503-29736554 | Rare:13 |