| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:778600-778819 | Common:4; Rare:93 | ||||
| chr1:827500-827721 | Common:2; Rare:86 | ||||
| chr1:12342841-12342981 | Rare:37 | ||||
| chr1:12619107-12619242 | Rare:30 | ||||
| chr1:15834840-15835134 | Common:2; Rare:131 | ||||
| chr1:16499217-16499538 | Common:3; Rare:124 | ||||
| chr1:16644637-16644790 | Common:1; Rare:2 | ||||
| chr1:16889401-16889536 | Common:4; Rare:28 | ||||
| chr1:16895602-16895725 | Common:2; Rare:26 | ||||
| chr1:16913883-16914119 | Common:8; Rare:48 | ||||
| chr1:21857176-21857325 | Common:1; Rare:40; Clinvar:2 | ||||
| chr1:21884865-21885149 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:28581869-28581984 | Common:1; Rare:35 | ||||
| chr1:28648308-28648600 | Common:4; Rare:84 | ||||
| chr1:31696248-31696499 | Common:2; Rare:47 |