| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:53242110-53242501 | Common:1; Rare:173 | ||||
| chr3:53255399-53255799 | Common:4; Rare:103 | ||||
| chr3:53255862-53256309 | Common:18; Rare:554 | ||||
| chr3:53346937-53347337 | Rare:79 | ||||
| chr3:53347440-53348201 | Common:16; Rare:697 | ||||
| chr3:53846201-53846730 | Common:5; Rare:842 | ||||
| chr3:53881380-53882043 | Common:11; Rare:274 | ||||
| chr3:53882051-53882451 | Common:13; Rare:312 | ||||
| chr3:53891720-53892151 | Common:28; Rare:704 | ||||
| chr3:55607741-55608141 | Common:2; Rare:66 | ||||
| chr3:56556936-56557336 | Common:23; Rare:576; Clinvar (benign):1 | ||||
| chr3:56557565-56557993 | Common:6; Rare:262 | ||||
| chr3:56558013-56558413 | Common:3; Rare:86 | ||||
| chr3:56682030-56683093 | Common:16; Rare:713 | ||||
| chr3:56683100-56683535 | Common:26; Rare:573 |