| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:6202732-6202946 | Common:4; Rare:58 | ||||
| chr10:6580246-6580561 | Common:11; Rare:102 | ||||
| chr10:7787957-7788232 | Common:1; Rare:114 | ||||
| chr10:12195838-12196234 | Rare:101 | ||||
| chr10:13099949-13100205 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):4 | ||||
| chr10:14008145-14008222 | Rare:31 | ||||
| chr10:14838017-14838337 | Common:2; Rare:85 | ||||
| chr10:14878645-14878879 | Common:2; Rare:69 | ||||
| chr10:17643898-17644241 | Common:2; Rare:102 | ||||
| chr10:18651596-18651732 | Common:1; Rare:53 | ||||
| chr10:18659254-18659603 | Common:2; Rare:118 | ||||
| chr10:22316220-22316458 | Common:1; Rare:109 | ||||
| chr10:24209015-24209178 | Rare:47 | ||||
| chr10:27154325-27154446 | Rare:32 | ||||
| chr10:27155203-27155376 | Common:4; Rare:57; Clinvar:2; Clinvar (benign):4 |