| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:88158810-88159530 | Common:11; Rare:357 | ||||
| chr4:88283320-88283710 | Rare:68 | ||||
| chr4:88283760-88284060 | Common:3; Rare:138 | ||||
| chr4:88284177-88285010 | Common:14; Rare:428 | ||||
| chr4:88378470-88379220 | Common:10; Rare:334 | ||||
| chr4:88379246-88379438 | Rare:49 | ||||
| chr4:88456894-88457177 | Common:5; Rare:158 | ||||
| chr4:88523662-88523926 | Common:7; Rare:192 | ||||
| chr4:88592249-88592550 | Common:3; Rare:238 | ||||
| chr4:88593007-88593437 | Common:8; Rare:176 | ||||
| chr4:88737650-88738200 | Common:1; Rare:95 | ||||
| chr4:88823159-88823550 | Common:4; Rare:133 | ||||
| chr4:89057030-89057340 | Common:3; Rare:63 | ||||
| chr4:89111281-89111695 | Common:12; Rare:396 | ||||
| chr4:89836950-89837570 | Common:5; Rare:186; Clinvar:4; Clinvar (benign):1 |