| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:16644644-16644805 | Common:1; Rare:3 | ||||
| chr1:16765274-16765494 | Rare:13 | ||||
| chr1:16889391-16889687 | Common:8; Rare:60 | ||||
| chr1:16895956-16895980 | Common:3; Rare:4 | ||||
| chr1:16904815-16904950 | Common:2; Rare:17 | ||||
| chr1:16913904-16914115 | Common:7; Rare:43 | ||||
| chr1:19404685-19404865 | Common:3; Rare:28 | ||||
| chr1:19418629-19418899 | Common:1; Rare:46 | ||||
| chr1:21827862-21828044 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:21855521-21855913 | Common:4; Rare:132; Clinvar:9; Clinvar (benign):5 | ||||
| chr1:21857015-21857325 | Common:1; Rare:96; Clinvar:5; Clinvar (benign):2 | ||||
| chr1:21859577-21859991 | Common:2; Rare:137; Clinvar:4 | ||||
| chr1:21873374-21873652 | Common:8; Rare:78; Clinvar:1 | ||||
| chr1:21876227-21876653 | Common:2; Rare:153; Clinvar:11; Clinvar (benign):2 | ||||
| chr1:21884765-21885151 | Common:1; Rare:117; Clinvar:2; Clinvar (benign):1 |