| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:150603168-150603299 | Common:1; Rare:40 | ||||
| chr3:179604636-179604810 | Common:1; Rare:49 | ||||
| chr3:196942398-196942659 | Common:1; Rare:103 | ||||
| chr3:197949907-197950240 | Common:3; Rare:100; Clinvar (benign):2 | ||||
| chr4:673849-673940 | Rare:40 | ||||
| chr4:674248-674497 | Rare:119 | ||||
| chr4:932302-932477 | Common:2; Rare:72 | ||||
| chr4:2041935-2042061 | Rare:56 | ||||
| chr4:6640537-6640697 | Common:2; Rare:63 | ||||
| chr4:57110085-57110205 | Rare:42 | ||||
| chr4:82373973-82374108 | Common:2; Rare:35 | ||||
| chr4:99088704-99088855 | Common:5; Rare:62 | ||||
| chr4:140373350-140373649 | Common:1; Rare:105 | ||||
| chr4:173370697-173370954 | Common:1; Rare:63 | ||||
| chr5:218149-218336 | Common:2; Rare:62; Clinvar:1; Clinvar (benign):2 |