| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:41918006-41918219 | Common:3; Rare:64 | ||||
| chr1:42035375-42035753 | Common:2; Rare:102 | ||||
| chr1:42035868-42036205 | Common:1; Rare:88 | ||||
| chr1:42335156-42335716 | Common:8; Rare:195 | ||||
| chr1:42335833-42335929 | Rare:17 | ||||
| chr1:42380587-42380840 | Common:1; Rare:83 | ||||
| chr1:42455927-42456114 | Common:1; Rare:73 | ||||
| chr1:42456206-42456651 | Common:3; Rare:148 | ||||
| chr1:42456839-42457038 | Common:1; Rare:71; Clinvar (pathogenic):1 | ||||
| chr1:42658026-42658144 | Rare:31 | ||||
| chr1:42658226-42658556 | Common:3; Rare:90 | ||||
| chr1:42681945-42682519 | Common:2; Rare:181 | ||||
| chr1:42682760-42682998 | Common:1; Rare:94 | ||||
| chr1:42683026-42683194 | Rare:86 | ||||
| chr1:42766908-42767351 | Common:6; Rare:158; Clinvar (benign):1; Clinvar (pathogenic):1 |