| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173369503-173369545 | Common:1; Rare:8 | ||||
| chr4:173369610-173370003 | Common:2; Rare:97 | ||||
| chr4:173370661-173371209 | Common:3; Rare:148 | ||||
| chr4:174283153-174283394 | Rare:39 | ||||
| chr4:174283601-174284074 | Common:1; Rare:106 | ||||
| chr4:176065726-176065904 | Common:2; Rare:58 | ||||
| chr4:176319713-176320079 | Common:5; Rare:121 | ||||
| chr4:176320209-176320355 | Rare:34 | ||||
| chr4:176320434-176320637 | Rare:56 | ||||
| chr4:177309727-177309948 | Common:2; Rare:70 | ||||
| chr4:177310249-177310355 | Rare:27 | ||||
| chr4:177442025-177442810 | Common:3; Rare:293; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr4:177442927-177443026 | Rare:19 | ||||
| chr4:182916798-182917025 | Common:2; Rare:40 | ||||
| chr4:182917278-182917646 | Common:4; Rare:113 |