| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:169270927-169271128 | Common:1; Rare:66 | ||||
| chr4:169612575-169612811 | Common:4; Rare:72; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:169620400-169620702 | Common:2; Rare:102 | ||||
| chr4:169660036-169660287 | Common:1; Rare:46 | ||||
| chr4:173168213-173168280 | Common:1; Rare:16 | ||||
| chr4:173168570-173168851 | Common:2; Rare:89 | ||||
| chr4:173334261-173334593 | Rare:94 | ||||
| chr4:173369741-173369955 | Common:1; Rare:71 | ||||
| chr4:173370681-173370976 | Common:2; Rare:76 | ||||
| chr4:174283594-174284032 | Common:1; Rare:96 | ||||
| chr4:174284262-174284364 | Common:1; Rare:25 | ||||
| chr4:176319721-176320124 | Common:5; Rare:128 | ||||
| chr4:176792213-176792425 | Rare:62 | ||||
| chr4:177442371-177442554 | Rare:108; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:182143894-182143975 | Rare:19 |