| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:87342264-87342414 | Common:3; Rare:47 | ||||
| chr10:87862256-87862570 | Rare:151; Clinvar:1 | ||||
| chr10:88939505-88939850 | Rare:62; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr10:96090197-96090319 | Common:1; Rare:53 | ||||
| chr10:103661093-103661361 | Common:1; Rare:69 | ||||
| chr10:103668718-103668844 | Rare:36 | ||||
| chr10:103678155-103678389 | Common:1; Rare:44 | ||||
| chr10:104336867-104336996 | Rare:24 | ||||
| chr10:113129163-113129301 | Common:1; Rare:29 | ||||
| chr11:309307-309472 | Rare:34 | ||||
| chr11:310107-310127 | Rare:3 | ||||
| chr11:311113-311299 | Common:1; Rare:13 | ||||
| chr11:319949-320130 | Common:1; Rare:57 | ||||
| chr11:1995874-1996202 | Common:1; Rare:94 | ||||
| chr11:1996280-1996439 | Rare:53 |