| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:44324635-44325032 | Common:4; Rare:125 | ||||
| chr17:44325317-44325510 | Common:3; Rare:40 | ||||
| chr17:44344988-44345364 | Common:1; Rare:86; Clinvar:5; Clinvar (benign):4 | ||||
| chr17:44345719-44345825 | Rare:13 | ||||
| chr17:44363764-44363862 | Common:1; Rare:29 | ||||
| chr17:44385298-44385632 | Common:4; Rare:111; Clinvar:1 | ||||
| chr17:44502689-44503024 | Common:3; Rare:74 | ||||
| chr17:44503173-44503773 | Common:1; Rare:213 | ||||
| chr17:44503829-44503858 | Rare:4 | ||||
| chr17:44556946-44557299 | Rare:69 | ||||
| chr17:44557315-44557597 | Common:2; Rare:69 | ||||
| chr17:44689352-44689533 | Rare:40 | ||||
| chr17:44689676-44690113 | Common:1; Rare:131 | ||||
| chr17:44708484-44708892 | Common:4; Rare:103 | ||||
| chr17:44775606-44775767 | Rare:38 |