| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:43410360-43410900 | Rare:91 | ||||
| chr3:43413968-43414296 | Rare:53 | ||||
| chr3:43423169-43423513 | Common:1; Rare:56 | ||||
| chr3:43565560-43566072 | Common:11; Rare:354; Clinvar (benign):1 | ||||
| chr3:45074510-45074780 | Common:3; Rare:46 | ||||
| chr3:45167540-45167850 | Common:6; Rare:105 | ||||
| chr3:45183180-45183700 | Common:9; Rare:178 | ||||
| chr3:45593236-45593430 | Common:2; Rare:41 | ||||
| chr3:45986290-45986790 | Common:1; Rare:89 | ||||
| chr3:46065270-46065800 | Common:4; Rare:90 | ||||
| chr3:46111120-46111442 | Common:8; Rare:191 | ||||
| chr3:46113926-46114630 | Common:6; Rare:192 | ||||
| chr3:46114613-46115151 | Common:2; Rare:193 | ||||
| chr3:46119770-46120812 | Common:12; Rare:252 | ||||
| chr3:46188744-46189016 | Common:1; Rare:54 |