| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:239927510-239927910 | Common:2; Rare:146 | ||||
| chr2:240370094-240370494 | Common:3; Rare:154 | ||||
| chr2:240387690-240388070 | Common:6; Rare:87 | ||||
| chr2:240426770-240427220 | Common:11; Rare:181 | ||||
| chr2:240434028-240434428 | Common:5; Rare:131 | ||||
| chr2:240434738-240435020 | Common:3; Rare:84 | ||||
| chr2:241953620-241954100 | Common:9; Rare:103 | ||||
| chr2:242088356-242088800 | Common:13; Rare:213 | ||||
| chr20:298212-298557 | Common:1; Rare:153 | ||||
| chr20:326010-326490 | Common:4; Rare:179 | ||||
| chr20:366090-366470 | Common:6; Rare:88 | ||||
| chr20:371854-372124 | Common:10; Rare:99 | ||||
| chr20:373435-373835 | Common:10; Rare:132 | ||||
| chr20:381857-382109 | Common:3; Rare:94 | ||||
| chr20:420370-421191 | Common:15; Rare:254; Clinvar (benign):3; Clinvar (pathogenic):1 |