| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:163494679-163494807 | Common:1; Rare:55 | ||||
| chr4:165112749-165112991 | Common:1; Rare:85 | ||||
| chr4:165207440-165207470 | Common:1; Rare:8 | ||||
| chr4:165327414-165327748 | Common:2; Rare:98 | ||||
| chr4:168318747-168318871 | Rare:26 | ||||
| chr4:168480416-168480511 | Common:1; Rare:18 | ||||
| chr4:169009998-169010160 | Common:3; Rare:48 | ||||
| chr4:169270880-169271162 | Common:2; Rare:93 | ||||
| chr4:169612496-169612771 | Common:6; Rare:96; Clinvar:5; Clinvar (benign):2 | ||||
| chr4:169620390-169620707 | Common:2; Rare:110 | ||||
| chr4:169660020-169660302 | Common:1; Rare:53 | ||||
| chr4:169757834-169758080 | Common:2; Rare:79 | ||||
| chr4:173168169-173168291 | Common:2; Rare:29 | ||||
| chr4:173168637-173168830 | Common:2; Rare:67 | ||||
| chr4:173334272-173334429 | Rare:51 |