| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2396738-2397148 | Common:6; Rare:266 | ||||
| chr17:2399483-2400061 | Common:6; Rare:314 | ||||
| chr17:2401005-2401368 | Common:1; Rare:297 | ||||
| chr17:2401461-2401722 | Common:2; Rare:140 | ||||
| chr17:2511463-2511684 | Rare:64 | ||||
| chr17:2511734-2512103 | Common:7; Rare:251 | ||||
| chr17:2592939-2593339 | Common:1; Rare:178 | ||||
| chr17:2593437-2593735 | Common:10; Rare:308; Clinvar:6; Clinvar (benign):6 | ||||
| chr17:2594053-2594222 | Rare:94 | ||||
| chr17:2710795-2711495 | Common:9; Rare:369 | ||||
| chr17:2711636-2712065 | Common:6; Rare:327 | ||||
| chr17:2776270-2777008 | Common:21; Rare:393 | ||||
| chr17:3557750-3558310 | Common:9; Rare:150; Clinvar:10; Clinvar (benign):9 | ||||
| chr17:3636177-3636607 | Common:17; Rare:349; Clinvar:2; Clinvar (benign):7 | ||||
| chr17:3636646-3636789 | Common:2; Rare:65; Clinvar:4; Clinvar (benign):2 |