| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:150235938-150236507 | Common:2; Rare:127 | ||||
| chr1:150256500-150256823 | Common:1; Rare:60 | ||||
| chr1:150256826-150256883 | Rare:7 | ||||
| chr1:150256902-150256919 | Rare:1 | ||||
| chr1:150257683-150257850 | Rare:40 | ||||
| chr1:150268915-150269201 | Rare:74 | ||||
| chr1:150272663-150272740 | Common:1; Rare:17 | ||||
| chr1:150281990-150282096 | Rare:28 | ||||
| chr1:150282104-150282597 | Common:3; Rare:112 | ||||
| chr1:150293727-150293943 | Common:2; Rare:74 | ||||
| chr1:150294058-150294161 | Common:1; Rare:22 | ||||
| chr1:150320834-150321003 | Common:2; Rare:29 | ||||
| chr1:150321382-150321712 | Rare:98; Clinvar:3; Clinvar (benign):1 | ||||
| chr1:150363581-150363759 | Common:1; Rare:56 | ||||
| chr1:150363891-150364325 | Common:4; Rare:132 |