| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:230426276-230426530 | Common:2; Rare:100 | ||||
| chr1:230572188-230572318 | Common:1; Rare:24 | ||||
| chr1:230702231-230702536 | Common:2; Rare:55; Clinvar (benign):1 | ||||
| chr1:230702631-230702938 | Common:1; Rare:59; Clinvar:4 | ||||
| chr1:230702965-230703191 | Common:1; Rare:64; Clinvar:2 | ||||
| chr1:230708606-230708918 | Common:2; Rare:71 | ||||
| chr1:230709014-230709126 | Common:1; Rare:25 | ||||
| chr1:230744525-230744719 | Rare:39 | ||||
| chr1:230745060-230745373 | Common:3; Rare:56 | ||||
| chr1:230751706-230751890 | Common:3; Rare:36 | ||||
| chr1:230867879-230867939 | Rare:13 | ||||
| chr1:230894594-230894739 | Rare:21 | ||||
| chr1:230899868-230900196 | Rare:67 | ||||
| chr1:230949041-230949225 | Common:4; Rare:28 | ||||
| chr1:230977965-230978225 | Common:3; Rare:58 |