| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:98517458-98517755 | Common:2; Rare:57 | ||||
| chr4:99013549-99013719 | Rare:36 | ||||
| chr4:99021630-99021781 | Common:1; Rare:35 | ||||
| chr4:113214412-113214737 | Common:4; Rare:51 | ||||
| chr4:113465546-113465682 | Rare:26 | ||||
| chr4:113758888-113758958 | Rare:13 | ||||
| chr4:118279101-118279190 | Common:3; Rare:23 | ||||
| chr4:118591655-118591868 | Rare:88 | ||||
| chr4:119128231-119128483 | Common:1; Rare:40 | ||||
| chr4:119136445-119136803 | Common:3; Rare:84; Clinvar:1; Clinvar (benign):8 | ||||
| chr4:119454577-119455024 | Common:17; Rare:143 | ||||
| chr4:121071285-121071348 | Rare:16 | ||||
| chr4:123827008-123827192 | Rare:33 | ||||
| chr4:125314774-125315186 | Common:4; Rare:107 | ||||
| chr4:131976160-131976271 | Common:3; Rare:41 |