| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:16817373-16817751 | Common:3; Rare:138 | ||||
| chr10:17201641-17201743 | Rare:31 | ||||
| chr10:18651582-18651778 | Common:1; Rare:79 | ||||
| chr10:22316227-22316500 | Common:2; Rare:127 | ||||
| chr10:22316931-22317188 | Common:1; Rare:51 | ||||
| chr10:22325513-22325666 | Rare:67 | ||||
| chr10:24208764-24209190 | Common:1; Rare:120 | ||||
| chr10:24466335-24466560 | Rare:34 | ||||
| chr10:27154354-27154474 | Rare:34 | ||||
| chr10:27155116-27155376 | Common:4; Rare:77; Clinvar:5; Clinvar (benign):4 | ||||
| chr10:29735789-29736098 | Common:3; Rare:68 | ||||
| chr10:32056383-32056506 | Common:1; Rare:51 | ||||
| chr10:32378767-32378887 | Common:1; Rare:18 | ||||
| chr10:32446022-32446239 | Common:1; Rare:103 | ||||
| chr10:32958160-32958474 | Common:2; Rare:121 |