| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:87342264-87342414 | Not yet | Common:3; Rare:47 | 153 | ||
| chr10:87862256-87862570 | Not yet | Rare:151; Clinvar:1 | 309 | ||
| chr10:88939505-88939850 | Not yet | Rare:62; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | 406 | ||
| chr10:96090197-96090319 | Not yet | Common:1; Rare:53 | 158 | ||
| chr10:103661093-103661361 | Not yet | Common:1; Rare:69 | 222 | ||
| chr10:103668718-103668844 | Not yet | Rare:36 | 238 | ||
| chr10:103678155-103678389 | Not yet | Common:1; Rare:44 | 315 | ||
| chr10:104336867-104336996 | Not yet | Rare:24 | 265 | ||
| chr10:113129163-113129301 | Not yet | Common:1; Rare:29 | 195 | ||
| chr11:309307-309472 | Not yet | Rare:34 | 297 | ||
| chr11:310107-310127 | Not yet | Rare:3 | 26 | ||
| chr11:311113-311299 | Not yet | Common:1; Rare:13 | 170 | ||
| chr11:319949-320130 | Not yet | Common:1; Rare:57 | 276 | ||
| chr11:1995874-1996202 | Not yet | Common:1; Rare:94 | 358 | ||
| chr11:1996280-1996439 | Not yet | Rare:53 | 213 |