| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:16129274-16129345 | Common:1; Rare:13 | ||||
| chr1:16159034-16159255 | Rare:38 | ||||
| chr1:16499212-16499417 | Common:1; Rare:95 | ||||
| chr1:16644646-16644773 | Common:1; Rare:2 | ||||
| chr1:16904800-16904978 | Common:2; Rare:23 | ||||
| chr1:16913926-16914115 | Common:7; Rare:38 | ||||
| chr1:18945283-18945561 | Common:4; Rare:54 | ||||
| chr1:19011125-19011369 | Common:2; Rare:47 | ||||
| chr1:21827861-21828044 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:21887266-21887584 | Common:2; Rare:121; Clinvar:9; Clinvar (benign):2 | ||||
| chr1:23748828-23749077 | Common:1; Rare:50 | ||||
| chr1:26351946-26352207 | Common:1; Rare:51 | ||||
| chr1:26863771-26864276 | Common:1; Rare:120 | ||||
| chr1:27489182-27489264 | Common:8; Rare:21 | ||||
| chr1:27540232-27540534 | Common:2; Rare:44 |