| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:32486403-32486784 | Common:1; Rare:132 | ||||
| chr17:32486799-32487165 | Common:1; Rare:139 | ||||
| chr17:32487840-32487919 | Rare:25 | ||||
| chr17:32877048-32877449 | Rare:114 | ||||
| chr17:32877639-32877690 | Rare:9 | ||||
| chr17:34961176-34961602 | Common:3; Rare:173 | ||||
| chr17:34980329-34980591 | Common:4; Rare:78 | ||||
| chr17:34980652-34980873 | Common:2; Rare:69 | ||||
| chr17:34981114-34981305 | Common:2; Rare:30 | ||||
| chr17:35063698-35063838 | Rare:22 | ||||
| chr17:35088762-35089057 | Common:1; Rare:59 | ||||
| chr17:35089179-35089624 | Common:7; Rare:103 | ||||
| chr17:35119131-35119293 | Rare:51; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:35119776-35119925 | Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:35141550-35141743 | Common:1; Rare:40 |