| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44170481-44170722 | Rare:46 | ||||
| chr17:44186623-44187041 | Common:1; Rare:147 | ||||
| chr17:44187169-44187274 | Rare:30 | ||||
| chr17:44221202-44221409 | Rare:58 | ||||
| chr17:44222085-44222321 | Rare:50 | ||||
| chr17:44324765-44324976 | Common:2; Rare:79 | ||||
| chr17:44345057-44345321 | Rare:55; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:44385313-44385580 | Common:4; Rare:81; Clinvar:1 | ||||
| chr17:44503363-44503727 | Rare:138 | ||||
| chr17:44557084-44557370 | Common:1; Rare:50 | ||||
| chr17:44758916-44759191 | Common:2; Rare:69 | ||||
| chr17:44899363-44899774 | Common:3; Rare:128; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:44911505-44911597 | Common:3; Rare:26; Clinvar:2 | ||||
| chr17:44947675-44947930 | Common:1; Rare:73 | ||||
| chr17:45051406-45051693 | Common:1; Rare:93 |