| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28717174-28717325 | Common:2; Rare:63 | ||||
| chr17:28717585-28717707 | Common:2; Rare:33 | ||||
| chr17:28717785-28718075 | Rare:58 | ||||
| chr17:28718087-28718212 | Rare:35 | ||||
| chr17:28719487-28719692 | Rare:47 | ||||
| chr17:28719926-28720130 | Rare:82 | ||||
| chr17:28720242-28720558 | Common:3; Rare:139 | ||||
| chr17:28723278-28723432 | Common:1; Rare:41 | ||||
| chr17:28725668-28726015 | Common:1; Rare:108 | ||||
| chr17:28726181-28726372 | Common:4; Rare:42 | ||||
| chr17:28727059-28727112 | Common:1; Rare:14 | ||||
| chr17:28727132-28727144 | Rare:2 | ||||
| chr17:28728718-28728840 | Rare:46; Clinvar (benign):1 | ||||
| chr17:28728868-28729131 | Common:2; Rare:70 | ||||
| chr17:28743784-28744096 | Common:4; Rare:89 |