| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2710770-2711109 | Common:1; Rare:87 | ||||
| chr17:2711165-2711352 | Common:2; Rare:50 | ||||
| chr17:2711636-2712041 | Common:2; Rare:111 | ||||
| chr17:2776594-2776934 | Common:6; Rare:102 | ||||
| chr17:2776936-2777007 | Rare:15 | ||||
| chr17:3474340-3474563 | Common:1; Rare:29 | ||||
| chr17:3530321-3530504 | Common:3; Rare:50 | ||||
| chr17:3530540-3530722 | Common:1; Rare:30 | ||||
| chr17:3530723-3530769 | Rare:8 | ||||
| chr17:3635547-3635914 | Common:3; Rare:83 | ||||
| chr17:3636172-3636514 | Common:4; Rare:108; Clinvar (benign):1 | ||||
| chr17:3636677-3636789 | Common:1; Rare:30; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:3667964-3668276 | Rare:70 | ||||
| chr17:3668391-3668906 | Common:3; Rare:205 | ||||
| chr17:3723691-3723999 | Common:1; Rare:168 |