| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:26320914-26321057 | Rare:52; Clinvar (benign):1 | ||||
| chr4:26860568-26860812 | Common:2; Rare:81 | ||||
| chr4:30721970-30722269 | Common:2; Rare:93 | ||||
| chr4:36243859-36244053 | Common:1; Rare:42 | ||||
| chr4:36244274-36244627 | Common:3; Rare:119 | ||||
| chr4:37826553-37826769 | Common:2; Rare:83 | ||||
| chr4:38664194-38664486 | Common:2; Rare:91 | ||||
| chr4:38867612-38867846 | Common:2; Rare:84 | ||||
| chr4:39182353-39182554 | Common:1; Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:39458857-39459112 | Common:3; Rare:147; Clinvar (benign):5 | ||||
| chr4:39527349-39527754 | Common:4; Rare:100 | ||||
| chr4:39638829-39639209 | Common:1; Rare:146 | ||||
| chr4:39697939-39698306 | Common:2; Rare:143 | ||||
| chr4:39698701-39698870 | Rare:34 | ||||
| chr4:40056605-40056944 | Common:4; Rare:104 |