| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52685536-52686187 | Common:4; Rare:218 | ||||
| chr3:52705557-52706217 | Common:4; Rare:210 | ||||
| chr3:52770907-52771075 | Common:2; Rare:47 | ||||
| chr3:53130405-53130533 | Common:1; Rare:40; Clinvar (benign):3 | ||||
| chr3:53347504-53347723 | Common:2; Rare:70 | ||||
| chr3:53891807-53892033 | Common:2; Rare:68 | ||||
| chr3:56557086-56557238 | Common:2; Rare:60 | ||||
| chr3:57227585-57227896 | Common:3; Rare:109 | ||||
| chr3:57555996-57556321 | Rare:81 | ||||
| chr3:57597286-57597683 | Common:4; Rare:124 | ||||
| chr3:58008271-58008527 | Common:2; Rare:96; Clinvar:5 | ||||
| chr3:58433805-58434046 | Common:2; Rare:84; Clinvar (benign):2 | ||||
| chr3:61251376-61251594 | Common:4; Rare:55 | ||||
| chr3:62318890-62319055 | Rare:69 | ||||
| chr3:63863747-63864114 | Common:7; Rare:120 |