| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:30831823-30832059 | Rare:74 | ||||
| chr17:30906182-30906379 | Common:1; Rare:64 | ||||
| chr17:30968681-30968798 | Rare:22 | ||||
| chr17:31859106-31859461 | Common:3; Rare:93 | ||||
| chr17:31901623-31901950 | Common:3; Rare:101 | ||||
| chr17:31936777-31937059 | Rare:81 | ||||
| chr17:32142372-32142620 | Common:8; Rare:110 | ||||
| chr17:32341861-32342022 | Rare:40 | ||||
| chr17:32342085-32342262 | Rare:51 | ||||
| chr17:32349981-32350245 | Rare:128 | ||||
| chr17:34961453-34961585 | Common:1; Rare:65 | ||||
| chr17:34980364-34980843 | Common:5; Rare:145 | ||||
| chr17:35063654-35063848 | Rare:32 | ||||
| chr17:35089109-35089503 | Common:5; Rare:92 | ||||
| chr17:35119598-35120068 | Common:1; Rare:153; Clinvar:10; Clinvar (benign):10; Clinvar (pathogenic):1 |