| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:5843072-5843100 | Rare:5 | ||||
| chr4:6673293-6673451 | Common:2; Rare:40 | ||||
| chr4:6673835-6674072 | Common:11; Rare:115 | ||||
| chr4:6783553-6783776 | Rare:73 | ||||
| chr4:8705195-8705278 | Common:3; Rare:14 | ||||
| chr4:15020660-15020755 | Common:1; Rare:15 | ||||
| chr4:16007767-16007950 | Common:1; Rare:24 | ||||
| chr4:16025056-16025266 | Common:1; Rare:50; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:16521367-16521632 | Rare:34 | ||||
| chr4:18319109-18319271 | Common:1; Rare:36 | ||||
| chr4:20951000-20951223 | Common:1; Rare:45 | ||||
| chr4:21076203-21076342 | Common:2; Rare:29 | ||||
| chr4:22997407-22997591 | Common:2; Rare:41 | ||||
| chr4:25977765-25978209 | Rare:86 | ||||
| chr4:26028829-26028917 | Rare:33 |