| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:18781121-18781305 | Common:3; Rare:51 | ||||
| chr17:18856187-18856362 | Common:1; Rare:29 | ||||
| chr17:19362575-19362773 | Common:2; Rare:91; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:19377887-19378029 | Common:1; Rare:36 | ||||
| chr17:19378162-19378560 | Common:2; Rare:94 | ||||
| chr17:19648665-19648797 | Common:2; Rare:44 | ||||
| chr17:19977796-19977958 | Common:1; Rare:55 | ||||
| chr17:21214144-21214351 | Common:2; Rare:93 | ||||
| chr17:27294353-27294392 | Rare:14 | ||||
| chr17:28335373-28335841 | Common:1; Rare:112 | ||||
| chr17:28357428-28357667 | Common:5; Rare:120 | ||||
| chr17:28598994-28599160 | Common:2; Rare:47 | ||||
| chr17:28645082-28645368 | Common:1; Rare:112 | ||||
| chr17:28661837-28661941 | Rare:50 | ||||
| chr17:28662166-28662303 | Rare:57 |