| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:2261798-2262792 | Common:14; Rare:695 | ||||
| chr4:2418460-2419120 | Common:18; Rare:425 | ||||
| chr4:2462160-2462700 | Common:2; Rare:150 | ||||
| chr4:2468798-2469220 | Common:13; Rare:424 | ||||
| chr4:2469608-2470008 | Common:1; Rare:147 | ||||
| chr4:2746210-2746673 | Rare:240 | ||||
| chr4:2755963-2756180 | Common:2; Rare:138 | ||||
| chr4:2756246-2756670 | Common:11; Rare:243 | ||||
| chr4:2792838-2793137 | Common:4; Rare:148 | ||||
| chr4:2811980-2812490 | Common:1; Rare:107 | ||||
| chr4:2817580-2817980 | Common:2; Rare:97 | ||||
| chr4:2818112-2818300 | Common:1; Rare:62 | ||||
| chr4:2818640-2818990 | Common:8; Rare:133; Clinvar (benign):5 | ||||
| chr4:2820520-2820890 | Common:6; Rare:193; Clinvar:6; Clinvar (benign):6 | ||||
| chr4:2842840-2843643 | Common:17; Rare:268 |