| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:4894957-4895240 | Rare:83 | ||||
| chr17:4899246-4899481 | Common:1; Rare:158; Clinvar:13; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr17:4939897-4940030 | Rare:46 | ||||
| chr17:4940044-4940348 | Common:1; Rare:83 | ||||
| chr17:4943220-4943511 | Common:1; Rare:105 | ||||
| chr17:4947649-4947684 | Rare:16 | ||||
| chr17:4947908-4948026 | Rare:31 | ||||
| chr17:4948942-4949177 | Common:2; Rare:82 | ||||
| chr17:4949857-4950145 | Common:1; Rare:64 | ||||
| chr17:4967720-4968250 | Common:3; Rare:176 | ||||
| chr17:4987079-4987191 | Rare:26 | ||||
| chr17:4987414-4987767 | Common:3; Rare:111 | ||||
| chr17:4997900-4998156 | Common:2; Rare:102; Clinvar (benign):1 | ||||
| chr17:5078431-5078542 | Common:1; Rare:33 | ||||
| chr17:5191832-5192112 | Common:2; Rare:89 |