| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:165112771-165113037 | Common:1; Rare:86 | ||||
| chr4:165207461-165207684 | Common:2; Rare:87 | ||||
| chr4:165327406-165327753 | Common:2; Rare:101 | ||||
| chr4:165378879-165379102 | Common:2; Rare:55 | ||||
| chr4:165379182-165379674 | Common:2; Rare:238 | ||||
| chr4:167233864-167234470 | Common:3; Rare:317 | ||||
| chr4:168318226-168318779 | Common:9; Rare:152 | ||||
| chr4:168480310-168480710 | Common:2; Rare:142 | ||||
| chr4:168630819-168631240 | Common:4; Rare:112 | ||||
| chr4:168631577-168631706 | Rare:39 | ||||
| chr4:168632047-168632389 | Rare:61 | ||||
| chr4:168831840-168832106 | Common:2; Rare:65 | ||||
| chr4:169010237-169010552 | Common:2; Rare:91 | ||||
| chr4:169270933-169271316 | Common:2; Rare:114 | ||||
| chr4:169612504-169612835 | Common:7; Rare:100; Clinvar:5; Clinvar (benign):2 |