| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:5420031-5420207 | Rare:70 | ||||
| chr17:5438837-5438994 | Rare:50 | ||||
| chr17:5486127-5486616 | Common:6; Rare:171 | ||||
| chr17:5486810-5486925 | Common:3; Rare:38 | ||||
| chr17:6640646-6641090 | Common:7; Rare:139 | ||||
| chr17:6651553-6651806 | Common:1; Rare:88 | ||||
| chr17:6690495-6690793 | Common:2; Rare:59 | ||||
| chr17:6713336-6713503 | Common:4; Rare:41; Clinvar (benign):3 | ||||
| chr17:6996026-6996049 | Rare:7 | ||||
| chr17:7012301-7012686 | Rare:132 | ||||
| chr17:7035791-7036091 | Rare:72 | ||||
| chr17:7114583-7115155 | Common:10; Rare:111 | ||||
| chr17:7176357-7176697 | Common:14; Rare:145 | ||||
| chr17:7219796-7219989 | Common:3; Rare:85; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr17:7223825-7224328 | Rare:178; Clinvar:14; Clinvar (benign):11; Clinvar (pathogenic):15 |