| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:23778281-23778492 | Common:9; Rare:110 | ||||
| chr1:23800750-23800947 | Common:1; Rare:65 | ||||
| chr1:23959607-23959854 | Common:2; Rare:66 | ||||
| chr1:24642966-24643335 | Common:2; Rare:115 | ||||
| chr1:25232442-25232657 | Rare:87 | ||||
| chr1:25247451-25247630 | Common:2; Rare:62 | ||||
| chr1:25338188-25338485 | Common:2; Rare:101 | ||||
| chr1:25819902-25820219 | Common:3; Rare:94 | ||||
| chr1:26067024-26067217 | Common:1; Rare:35 | ||||
| chr1:26067318-26067850 | Common:4; Rare:112; Clinvar (benign):1 | ||||
| chr1:26182426-26182539 | Common:1; Rare:47 | ||||
| chr1:26234384-26234516 | Common:2; Rare:47 | ||||
| chr1:26257319-26257526 | Common:4; Rare:32 | ||||
| chr1:26279926-26280182 | Rare:142 | ||||
| chr1:26432100-26432403 | Common:5; Rare:82; Clinvar:2; Clinvar (benign):1 |