| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7043578-7043630 | Common:1; Rare:22 | ||||
| chr17:7043778-7044092 | Common:3; Rare:63 | ||||
| chr17:7219811-7219971 | Common:3; Rare:75; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:7222531-7222675 | Common:2; Rare:45; Clinvar (pathogenic):2 | ||||
| chr17:7223306-7223365 | Rare:18 | ||||
| chr17:7223953-7224243 | Rare:109; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):10 | ||||
| chr17:7224318-7224909 | Common:4; Rare:214; Clinvar:16; Clinvar (benign):25; Clinvar (pathogenic):4 | ||||
| chr17:7234446-7234650 | Common:2; Rare:104 | ||||
| chr17:7241767-7241934 | Common:2; Rare:36 | ||||
| chr17:7242100-7242207 | Common:1; Rare:19 | ||||
| chr17:7242234-7242618 | Common:1; Rare:115 | ||||
| chr17:7242958-7243121 | Common:1; Rare:86 | ||||
| chr17:7247062-7247289 | Common:2; Rare:61 | ||||
| chr17:7251963-7252700 | Common:4; Rare:274 | ||||
| chr17:7261111-7261214 | Common:1; Rare:24 |