| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:13749188-13749460 | Common:2; Rare:98 | ||||
| chr1:15526553-15526913 | Common:2; Rare:115 | ||||
| chr1:15736023-15736314 | Common:3; Rare:57 | ||||
| chr1:16017763-16018181 | Common:6; Rare:156 | ||||
| chr1:16352411-16352608 | Common:3; Rare:106 | ||||
| chr1:17053983-17054336 | Common:3; Rare:105; Clinvar:10; Clinvar (benign):9 | ||||
| chr1:17618208-17618419 | Common:2; Rare:49 | ||||
| chr1:19210234-19210433 | Rare:77 | ||||
| chr1:19251508-19251835 | Common:6; Rare:107 | ||||
| chr1:19312006-19312333 | Common:8; Rare:157 | ||||
| chr1:19596815-19597064 | Common:3; Rare:101 | ||||
| chr1:20661340-20661709 | Common:3; Rare:133; Clinvar:4; Clinvar (benign):6 | ||||
| chr1:21176878-21177092 | Rare:49 | ||||
| chr1:21345454-21345655 | Common:2; Rare:75 | ||||
| chr1:21854752-21854872 | Common:2; Rare:40; Clinvar:1; Clinvar (benign):1 |