| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:32143124-32143299 | Common:3; Rare:35 | ||||
| chr17:32341860-32342020 | Rare:58 | ||||
| chr17:32342097-32342288 | Rare:76 | ||||
| chr17:32349996-32350224 | Rare:211 | ||||
| chr17:32444400-32444540 | Rare:113 | ||||
| chr17:34255150-34255285 | Rare:37 | ||||
| chr17:34961412-34961575 | Common:2; Rare:138 | ||||
| chr17:34980221-34980625 | Common:8; Rare:174 | ||||
| chr17:34981120-34981534 | Common:3; Rare:125 | ||||
| chr17:35063653-35063838 | Rare:30 | ||||
| chr17:35089186-35089417 | Common:8; Rare:105 | ||||
| chr17:35119100-35119534 | Common:2; Rare:184; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):3 | ||||
| chr17:35119609-35119983 | Rare:211; Clinvar:9; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr17:35242891-35243145 | Rare:150 | ||||
| chr17:35373605-35373841 | Common:7; Rare:81 |