| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121801263-121801405 | Common:2; Rare:47 | ||||
| chr4:122152194-122152429 | Common:2; Rare:93 | ||||
| chr4:122732408-122732776 | Common:3; Rare:114; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:122826360-122826724 | Common:2; Rare:96 | ||||
| chr4:122922929-122923137 | Common:2; Rare:62 | ||||
| chr4:123399348-123399654 | Common:1; Rare:92 | ||||
| chr4:127632745-127633005 | Common:1; Rare:63 | ||||
| chr4:127782117-127782379 | Common:2; Rare:79 | ||||
| chr4:128060994-128061384 | Common:1; Rare:133 | ||||
| chr4:128287789-128287965 | Common:2; Rare:73 | ||||
| chr4:128811136-128811341 | Rare:46 | ||||
| chr4:129093431-129093736 | Common:2; Rare:85 | ||||
| chr4:133149105-133149295 | Common:2; Rare:54 | ||||
| chr4:139084192-139084543 | Common:4; Rare:156 | ||||
| chr4:139177189-139177437 | Rare:72 |