| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:108747092-108747176 | Common:3; Rare:20 | ||||
| chr1:108876793-108877196 | Common:2; Rare:111; Clinvar:7; Clinvar (benign):1 | ||||
| chr1:108963064-108963288 | Common:3; Rare:56 | ||||
| chr1:108963340-108963624 | Common:1; Rare:100 | ||||
| chr1:109041048-109041489 | Common:3; Rare:95 | ||||
| chr1:109041970-109042410 | Common:4; Rare:117 | ||||
| chr1:109075861-109076292 | Common:2; Rare:144 | ||||
| chr1:109090584-109091254 | Common:5; Rare:182 | ||||
| chr1:109213726-109214064 | Rare:113 | ||||
| chr1:109214299-109214497 | Common:1; Rare:39 | ||||
| chr1:109249483-109249616 | Rare:57 | ||||
| chr1:109283093-109283419 | Common:2; Rare:75 | ||||
| chr1:109283424-109283595 | Common:2; Rare:36 | ||||
| chr1:109397869-109398230 | Common:1; Rare:110 | ||||
| chr1:109425758-109425840 | Common:1; Rare:7 |