| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:107965020-107965520 | Common:2; Rare:313 | ||||
| chr1:108199710-108200040 | Common:2; Rare:127 | ||||
| chr1:108200066-108200529 | Common:19; Rare:267 | ||||
| chr1:108200849-108200955 | Common:1; Rare:26 | ||||
| chr1:108559846-108560415 | Common:11; Rare:426 | ||||
| chr1:108660992-108661474 | Common:13; Rare:410 | ||||
| chr1:108661500-108661890 | Common:2; Rare:155 | ||||
| chr1:108692128-108693212 | Common:13; Rare:795 | ||||
| chr1:108746339-108746783 | Common:4; Rare:198 | ||||
| chr1:108746871-108747113 | Rare:81 | ||||
| chr1:108830340-108831000 | Common:11; Rare:299 | ||||
| chr1:108876790-108877174 | Common:2; Rare:106; Clinvar:7; Clinvar (benign):1 | ||||
| chr1:108914168-108915234 | Common:12; Rare:294; Clinvar:1; Clinvar (benign):2 | ||||
| chr1:108962910-108963290 | Common:4; Rare:77 | ||||
| chr1:108963248-108963647 | Common:7; Rare:326 |