| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44219480-44219876 | Rare:143 | ||||
| chr17:44220439-44220714 | Common:3; Rare:108 | ||||
| chr17:44220801-44220978 | Rare:54 | ||||
| chr17:44221006-44221216 | Common:1; Rare:73 | ||||
| chr17:44221241-44221502 | Common:1; Rare:72 | ||||
| chr17:44222067-44222328 | Rare:55 | ||||
| chr17:44324752-44325036 | Common:2; Rare:101 | ||||
| chr17:44325335-44325546 | Common:3; Rare:45 | ||||
| chr17:44344995-44345346 | Common:1; Rare:77; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:44345382-44345656 | Common:1; Rare:52 | ||||
| chr17:44385301-44385596 | Common:4; Rare:91; Clinvar:1 | ||||
| chr17:44503161-44503797 | Common:1; Rare:218 | ||||
| chr17:44689673-44690115 | Common:1; Rare:133 | ||||
| chr17:44708459-44708732 | Common:2; Rare:51 | ||||
| chr17:44708755-44708913 | Common:3; Rare:56 |