| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:137448-137735 | Common:1; Rare:61 | ||||
| chr4:393082-393112 | Rare:2 | ||||
| chr4:480534-480857 | Common:1; Rare:73 | ||||
| chr4:527866-528139 | Common:2; Rare:43 | ||||
| chr4:672460-672560 | Common:1; Rare:36 | ||||
| chr4:1580258-1580524 | Common:3; Rare:58 | ||||
| chr4:1806081-1806323 | Common:2; Rare:93; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr4:1964891-1964994 | Rare:17 | ||||
| chr4:2254220-2254499 | Common:1; Rare:64 | ||||
| chr4:2856608-2856873 | Rare:54 | ||||
| chr4:2906287-2906567 | Common:1; Rare:60 | ||||
| chr4:2935519-2935871 | Common:3; Rare:81 | ||||
| chr4:2936044-2936341 | Common:2; Rare:72 | ||||
| chr4:2940202-2940420 | Common:3; Rare:52 | ||||
| chr4:2944131-2944339 | Common:1; Rare:64 |