| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52239063-52239249 | Common:2; Rare:66 | ||||
| chr3:52455464-52455630 | Common:2; Rare:54 | ||||
| chr3:52536330-52536609 | Common:2; Rare:79 | ||||
| chr3:52685960-52686033 | Common:1; Rare:23 | ||||
| chr3:52705565-52706195 | Common:4; Rare:201 | ||||
| chr3:56557086-56557203 | Common:2; Rare:40 | ||||
| chr3:57227598-57227845 | Common:2; Rare:87 | ||||
| chr3:57556006-57556331 | Rare:78 | ||||
| chr3:57597331-57597752 | Common:4; Rare:123 | ||||
| chr3:62318890-62319062 | Rare:71 | ||||
| chr3:63863752-63864158 | Common:8; Rare:135 | ||||
| chr3:67654591-67654727 | Common:1; Rare:51 | ||||
| chr3:69084762-69085050 | Common:3; Rare:71 | ||||
| chr3:88058932-88059255 | Common:3; Rare:103 | ||||
| chr3:97764485-97764795 | Common:1; Rare:65; Clinvar (benign):1 |