| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:127782516-127783498 | Common:12; Rare:511 | ||||
| chr4:127880100-127881005 | Common:7; Rare:623 | ||||
| chr4:127880975-127881776 | Common:3; Rare:626; Clinvar:2 | ||||
| chr4:127964711-127965111 | Common:1; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:127965077-127965949 | Common:32; Rare:889; Clinvar:16; Clinvar (benign):12 | ||||
| chr4:127965870-127966240 | Common:3; Rare:135; Clinvar (benign):4 | ||||
| chr4:128060900-128061620 | Common:7; Rare:1045 | ||||
| chr4:128286532-128286727 | Rare:59 | ||||
| chr4:128287139-128287539 | Common:1; Rare:144 | ||||
| chr4:128287621-128288081 | Common:11; Rare:479; Clinvar:1 | ||||
| chr4:128288060-128288529 | Common:32; Rare:548 | ||||
| chr4:128288860-128289020 | Rare:60 | ||||
| chr4:128809425-128810037 | Common:7; Rare:439 | ||||
| chr4:128810020-128810236 | Common:2; Rare:88 | ||||
| chr4:128810283-128810939 | Common:1; Rare:189 |