| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:65147990-65148214 | Common:8; Rare:96 | ||||
| chr1:65148637-65149024 | Common:8; Rare:248 | ||||
| chr1:65247976-65248253 | Rare:42 | ||||
| chr1:65254349-65254615 | Common:2; Rare:158 | ||||
| chr1:65309012-65310129 | Common:7; Rare:438 | ||||
| chr1:65420061-65420776 | Common:14; Rare:339; Clinvar:4; Clinvar (benign):2 | ||||
| chr1:66534062-66534766 | Common:11; Rare:240 | ||||
| chr1:66924770-66925060 | Common:4; Rare:332 | ||||
| chr1:66925125-66925534 | Common:6; Rare:246 | ||||
| chr1:66929901-66930420 | Common:1; Rare:339 | ||||
| chr1:66930580-66931100 | Common:4; Rare:273 | ||||
| chr1:67053397-67053808 | Common:6; Rare:194 | ||||
| chr1:67053910-67054435 | Common:8; Rare:337 | ||||
| chr1:67430268-67430737 | Rare:403 | ||||
| chr1:67684919-67685600 | Common:6; Rare:344 |