| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7573599-7573651 | Common:1; Rare:18 | ||||
| chr17:7573677-7573712 | Rare:12 | ||||
| chr17:7579576-7579706 | Rare:44 | ||||
| chr17:7582901-7583100 | Rare:60 | ||||
| chr17:7583102-7583191 | Rare:22 | ||||
| chr17:7583474-7583920 | Common:1; Rare:174; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:7584024-7584181 | Rare:39 | ||||
| chr17:7614546-7614669 | Rare:33 | ||||
| chr17:7614744-7614909 | Rare:47 | ||||
| chr17:7615006-7615409 | Rare:115 | ||||
| chr17:7627240-7627616 | Common:1; Rare:108 | ||||
| chr17:7627778-7628027 | Common:2; Rare:75 | ||||
| chr17:7650676-7650950 | Common:2; Rare:76 | ||||
| chr17:7686017-7686762 | Rare:206 | ||||
| chr17:7687430-7687666 | Rare:51; Clinvar:2 |