| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:195692358-195692434 | Rare:1 | ||||
| chr4:1200437-1200667 | Rare:52 | ||||
| chr4:1202312-1202586 | Common:2; Rare:62 | ||||
| chr4:6673844-6674099 | Common:11; Rare:124 | ||||
| chr4:12640341-12640415 | Common:3; Rare:17 | ||||
| chr4:38905517-38905834 | Common:1; Rare:107 | ||||
| chr4:51859384-51859560 | Rare:36 | ||||
| chr4:54231870-54232065 | Common:2; Rare:46 | ||||
| chr4:55398134-55398297 | Common:1; Rare:32 | ||||
| chr4:55947988-55948226 | Common:1; Rare:44 | ||||
| chr4:56490329-56490646 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):3 | ||||
| chr4:68337379-68337846 | Rare:153 | ||||
| chr4:68376585-68376639 | Rare:10 | ||||
| chr4:70688996-70689289 | Common:1; Rare:94 | ||||
| chr4:75725167-75725260 | Common:1; Rare:29 |