| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:73737429-73737713 | Rare:47 | ||||
| chr10:73743002-73743116 | Common:1; Rare:19 | ||||
| chr10:73769709-73770242 | Common:1; Rare:139 | ||||
| chr10:73912163-73912382 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:73912926-73913515 | Common:2; Rare:163; Clinvar:4; Clinvar (benign):1 | ||||
| chr10:73914710-73915175 | Common:1; Rare:108; Clinvar (benign):1 | ||||
| chr10:73917478-73917627 | Rare:26; Clinvar:1 | ||||
| chr10:73999145-73999289 | Rare:34 | ||||
| chr10:73999298-73999569 | Common:1; Rare:43 | ||||
| chr10:74002852-74003066 | Common:2; Rare:35 | ||||
| chr10:74009601-74009904 | Common:2; Rare:61 | ||||
| chr10:74035154-74035243 | Rare:17 | ||||
| chr10:74035794-74036068 | Common:1; Rare:46 | ||||
| chr10:74068569-74068717 | Common:1; Rare:25 | ||||
| chr10:74108967-74109448 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):2 |