| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:20254148-20254258 | Common:1; Rare:21 | ||||
| chr4:24584313-24584710 | Common:1; Rare:127 | ||||
| chr4:25160385-25160727 | Common:3; Rare:97; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233862-25234106 | Rare:102 | ||||
| chr4:25396674-25396910 | Rare:59 | ||||
| chr4:25914051-25914321 | Common:2; Rare:115 | ||||
| chr4:26320532-26321045 | Common:1; Rare:184; Clinvar (benign):1 | ||||
| chr4:26420802-26421005 | Common:1; Rare:29 | ||||
| chr4:26857515-26857762 | Common:4; Rare:74 | ||||
| chr4:26860568-26860854 | Common:3; Rare:98 | ||||
| chr4:26861272-26861359 | Rare:38 | ||||
| chr4:30720025-30720425 | Common:2; Rare:87 | ||||
| chr4:30723496-30723784 | Rare:69 | ||||
| chr4:37826349-37826769 | Common:8; Rare:133 | ||||
| chr4:38664208-38664291 | Rare:28 |