| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45060941-45061351 | Common:3; Rare:110 | ||||
| chr17:45104700-45104984 | Common:1; Rare:51 | ||||
| chr17:45132318-45132656 | Common:3; Rare:99 | ||||
| chr17:45148130-45148641 | Common:1; Rare:169 | ||||
| chr17:45161476-45161633 | Rare:47 | ||||
| chr17:45230943-45231130 | Rare:24 | ||||
| chr17:45316978-45317346 | Common:5; Rare:93 | ||||
| chr17:45490719-45490896 | Rare:58 | ||||
| chr17:45620218-45620362 | Rare:35 | ||||
| chr17:45894278-45894610 | Common:3; Rare:96; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:46193357-46193604 | Common:3; Rare:65 | ||||
| chr17:46225349-46225448 | Common:1; Rare:29 | ||||
| chr17:46922837-46923187 | Common:4; Rare:98; Clinvar:1; Clinvar (benign):7 | ||||
| chr17:47189156-47189591 | Common:1; Rare:115 | ||||
| chr17:47323861-47323987 | Common:2; Rare:42 |