| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:68721082-68721259 | Common:1; Rare:53 | ||||
| chr10:68721422-68721720 | Common:5; Rare:130 | ||||
| chr10:68827406-68827564 | Common:3; Rare:115 | ||||
| chr10:68901044-68901426 | Common:6; Rare:281 | ||||
| chr10:68956018-68957110 | Common:9; Rare:408 | ||||
| chr10:69179899-69180354 | Common:6; Rare:293 | ||||
| chr10:69416683-69416810 | Common:1; Rare:22 | ||||
| chr10:69416885-69417068 | Common:6; Rare:94 | ||||
| chr10:69451311-69451572 | Common:4; Rare:136 | ||||
| chr10:70132727-70133030 | Common:2; Rare:72 | ||||
| chr10:70146561-70146872 | Common:1; Rare:85 | ||||
| chr10:70170427-70170776 | Common:7; Rare:204 | ||||
| chr10:70233325-70233601 | Common:11; Rare:193; Clinvar (benign):1 | ||||
| chr10:70403971-70404218 | Rare:178 | ||||
| chr10:70404270-70404780 | Common:6; Rare:211 |