| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:174284262-174284349 | Common:1; Rare:20 | ||||
| chr4:174522416-174522537 | Rare:41; Clinvar (pathogenic):1 | ||||
| chr4:174829158-174829426 | Common:1; Rare:61 | ||||
| chr4:175812199-175812363 | Common:11; Rare:53 | ||||
| chr4:175812369-175812850 | Rare:94 | ||||
| chr4:176002315-176002524 | Rare:56 | ||||
| chr4:176065714-176066035 | Common:7; Rare:99 | ||||
| chr4:176195575-176195735 | Common:1; Rare:62 | ||||
| chr4:176319721-176320028 | Common:4; Rare:102 | ||||
| chr4:177309773-177309881 | Common:1; Rare:33 | ||||
| chr4:177442377-177442530 | Rare:92; Clinvar:2 | ||||
| chr4:182143819-182144138 | Common:5; Rare:70 | ||||
| chr4:182144181-182144203 | Rare:8 | ||||
| chr4:182144408-182144734 | Common:3; Rare:107 | ||||
| chr4:182448703-182449060 | Common:3; Rare:116 |