| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:40257867-40258287 | Common:4; Rare:114; Clinvar:8; Clinvar (benign):1 | ||||
| chr1:40450051-40450145 | Common:1; Rare:35 | ||||
| chr1:40508649-40508816 | Common:4; Rare:46 | ||||
| chr1:40531509-40531749 | Common:1; Rare:60 | ||||
| chr1:40691532-40691860 | Common:2; Rare:148 | ||||
| chr1:40692039-40692232 | Common:1; Rare:60 | ||||
| chr1:40709178-40709369 | Rare:48 | ||||
| chr1:40979457-40979806 | Common:4; Rare:112 | ||||
| chr1:42335164-42335351 | Common:3; Rare:96 | ||||
| chr1:42455993-42456110 | Rare:41 | ||||
| chr1:42456473-42456590 | Rare:59 | ||||
| chr1:42658275-42658482 | Common:2; Rare:62 | ||||
| chr1:42682158-42682442 | Common:2; Rare:71 | ||||
| chr1:42766978-42767312 | Common:4; Rare:115; Clinvar (benign):1 | ||||
| chr1:42817009-42817141 | Common:1; Rare:35 |