| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:22317027-22317148 | Rare:24 | ||||
| chr10:22321138-22321615 | Common:1; Rare:151 | ||||
| chr10:22325506-22325852 | Rare:138 | ||||
| chr10:22326272-22326461 | Common:1; Rare:46 | ||||
| chr10:22327304-22327646 | Rare:81 | ||||
| chr10:22345388-22345557 | Common:1; Rare:42 | ||||
| chr10:22714374-22714797 | Rare:166 | ||||
| chr10:22927918-22928102 | Common:2; Rare:69 | ||||
| chr10:23344034-23344088 | Common:1; Rare:12 | ||||
| chr10:24208780-24209206 | Common:1; Rare:120 | ||||
| chr10:24495012-24495196 | Common:1; Rare:46 | ||||
| chr10:25016106-25016677 | Common:11; Rare:170 | ||||
| chr10:25934373-25934486 | Common:2; Rare:35 | ||||
| chr10:26697591-26697643 | Rare:13 | ||||
| chr10:26697705-26697965 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):2 |