| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121823864-121824075 | Common:2; Rare:53 | ||||
| chr4:122152188-122152383 | Common:2; Rare:80 | ||||
| chr4:122732436-122732768 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922902-122923139 | Common:2; Rare:68 | ||||
| chr4:123399368-123399656 | Common:1; Rare:89 | ||||
| chr4:127880791-127880934 | Rare:49 | ||||
| chr4:128061000-128061380 | Common:1; Rare:130 | ||||
| chr4:128287796-128288058 | Common:3; Rare:98 | ||||
| chr4:128811062-128811317 | Rare:51 | ||||
| chr4:129093481-129093748 | Common:1; Rare:82 | ||||
| chr4:129096065-129096182 | Common:1; Rare:29 | ||||
| chr4:137532376-137532704 | Common:2; Rare:56 | ||||
| chr4:138242250-138242574 | Common:1; Rare:69 | ||||
| chr4:139301295-139301593 | Common:4; Rare:92 | ||||
| chr4:139453683-139453749 | Common:2; Rare:21 |