| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:58332658-58333346 | Common:22; Rare:319 | ||||
| chr3:58333261-58334044 | Common:9; Rare:288 | ||||
| chr3:58433353-58434130 | Common:11; Rare:750; Clinvar:11; Clinvar (benign):20 | ||||
| chr3:58491670-58492160 | Common:13; Rare:473 | ||||
| chr3:59049885-59050360 | Common:3; Rare:421 | ||||
| chr3:61250488-61250901 | Common:5; Rare:136 | ||||
| chr3:61251339-61251739 | Common:28; Rare:429 | ||||
| chr3:63863306-63863779 | Common:4; Rare:217 | ||||
| chr3:63863710-63864957 | Common:60; Rare:1631 | ||||
| chr3:63911710-63912200 | Rare:357 | ||||
| chr3:63912240-63912903 | Common:8; Rare:678; Clinvar (benign):4 | ||||
| chr3:63967511-63968736 | Common:7; Rare:448 | ||||
| chr3:64012474-64012874 | Common:7; Rare:163 | ||||
| chr3:64023380-64023730 | Common:10; Rare:354 | ||||
| chr3:64685770-64686180 | Common:1; Rare:87 |