| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:133276747-133276905 | Common:1; Rare:41 | ||||
| chr10:133308830-133308989 | Rare:74 | ||||
| chr10:133309077-133309163 | Rare:31 | ||||
| chr10:133357675-133357848 | Common:1; Rare:29 | ||||
| chr10:133357903-133358041 | Common:2; Rare:44 | ||||
| chr10:133373290-133373583 | Common:2; Rare:126; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr10:133378957-133379320 | Common:19; Rare:75 | ||||
| chr10:133379497-133379711 | Rare:47 | ||||
| chr10:133394077-133394425 | Rare:140 | ||||
| chr10:133401195-133401406 | Common:1; Rare:41 | ||||
| chr10:133520257-133520499 | Common:3; Rare:76 | ||||
| chr11:207335-207802 | Common:9; Rare:146 | ||||
| chr11:208586-208862 | Common:1; Rare:96 | ||||
| chr11:236217-236588 | Common:9; Rare:136 | ||||
| chr11:236801-237057 | Common:3; Rare:92 |