| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:241848121-241848270 | Common:1; Rare:24 | ||||
| chr1:243254629-243254952 | Common:2; Rare:97 | ||||
| chr1:243255040-243255448 | Common:1; Rare:98 | ||||
| chr1:243255729-243256117 | Rare:105; Clinvar:4 | ||||
| chr1:243417802-243417833 | Rare:4 | ||||
| chr1:243851166-243851226 | Common:2; Rare:22 | ||||
| chr1:243851228-243851281 | Common:1; Rare:15 | ||||
| chr1:244048233-244048552 | Rare:101 | ||||
| chr1:244050953-244051120 | Rare:31 | ||||
| chr1:244051140-244051416 | Common:1; Rare:40 | ||||
| chr1:244451840-244452060 | Rare:71 | ||||
| chr1:244835215-244835350 | Rare:48 | ||||
| chr1:244835580-244835747 | Common:2; Rare:76; Clinvar (benign):5 | ||||
| chr1:244862990-244863318 | Common:4; Rare:134 | ||||
| chr1:244863961-244864260 | Common:1; Rare:87; Clinvar:3; Clinvar (benign):6 |