| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:38853637-38853996 | Common:11; Rare:310 | ||||
| chr17:38869788-38870253 | Common:10; Rare:347 | ||||
| chr17:38870482-38870764 | Common:1; Rare:59 | ||||
| chr17:38967371-38967658 | Common:4; Rare:229 | ||||
| chr17:39197534-39197802 | Common:1; Rare:160 | ||||
| chr17:39199894-39200383 | Common:9; Rare:426 | ||||
| chr17:39200456-39200620 | Common:2; Rare:46 | ||||
| chr17:39401553-39401848 | Common:3; Rare:220 | ||||
| chr17:39402482-39402751 | Common:1; Rare:195 | ||||
| chr17:39451095-39451519 | Common:12; Rare:275 | ||||
| chr17:39461194-39461579 | Common:5; Rare:243 | ||||
| chr17:39461820-39462130 | Common:6; Rare:178 | ||||
| chr17:39636966-39637323 | Common:12; Rare:244 | ||||
| chr17:39637250-39637368 | Common:1; Rare:44 | ||||
| chr17:39687610-39687950 | Rare:169; Clinvar:2; Clinvar (pathogenic):2 |