| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:151408909-151409287 | Common:4; Rare:119 | ||||
| chr4:152779715-152780013 | Common:1; Rare:83 | ||||
| chr4:158172360-158172684 | Rare:50 | ||||
| chr4:158210347-158210567 | Common:3; Rare:54 | ||||
| chr4:158671858-158672444 | Common:5; Rare:150; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:164977586-164977738 | Rare:42 | ||||
| chr4:168831907-168832115 | Common:3; Rare:56 | ||||
| chr4:168894370-168894677 | Rare:63; Clinvar:2; Clinvar (benign):3 | ||||
| chr4:169620267-169620725 | Common:2; Rare:153 | ||||
| chr4:169660036-169660272 | Common:1; Rare:43 | ||||
| chr4:173333640-173333867 | Common:1; Rare:61 | ||||
| chr4:173369778-173369935 | Common:1; Rare:51 | ||||
| chr4:173370674-173370976 | Common:2; Rare:78 | ||||
| chr4:173399187-173399504 | Common:8; Rare:52 | ||||
| chr4:173530145-173530727 | Common:3; Rare:116 |