| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:121183661-121183957 | Common:1; Rare:55 | ||||
| chr1:121183993-121184118 | Rare:35 | ||||
| chr1:121184654-121185091 | Common:3; Rare:141 | ||||
| chr1:145093675-145093692 | Rare:2 | ||||
| chr1:145094973-145095008 | Rare:2 | ||||
| chr1:145215216-145215294 | Rare:6 | ||||
| chr1:145608277-145608322 | Common:1; Rare:16 | ||||
| chr1:145823841-145824308 | Rare:161 | ||||
| chr1:145824407-145824544 | Rare:31 | ||||
| chr1:145845593-145845710 | Common:1; Rare:50 | ||||
| chr1:145858883-145859406 | Common:1; Rare:144 | ||||
| chr1:145859621-145859958 | Common:2; Rare:89 | ||||
| chr1:145918649-145919057 | Common:2; Rare:99; Clinvar:1 | ||||
| chr1:145926887-145927016 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr1:145927335-145927737 | Common:1; Rare:108; Clinvar (pathogenic):1 |