| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:2934761-2934954 | Common:5; Rare:87 | ||||
| chr4:2942191-2942474 | Common:1; Rare:106 | ||||
| chr4:2962862-2962973 | Rare:28 | ||||
| chr4:2963295-2963639 | Common:3; Rare:134 | ||||
| chr4:3074500-3074728 | Common:5; Rare:75 | ||||
| chr4:3292804-3293079 | Common:2; Rare:112 | ||||
| chr4:3532211-3532615 | Common:2; Rare:183; Clinvar (pathogenic):2 | ||||
| chr4:4248062-4248281 | Common:5; Rare:113 | ||||
| chr4:4289976-4290319 | Common:5; Rare:115 | ||||
| chr4:4348811-4348920 | Common:1; Rare:20 | ||||
| chr4:4541733-4541824 | Common:1; Rare:37 | ||||
| chr4:4541878-4542347 | Common:5; Rare:167 | ||||
| chr4:5051366-5051909 | Common:5; Rare:182 | ||||
| chr4:5203907-5204055 | Common:2; Rare:35 | ||||
| chr4:5437843-5437985 | Common:4; Rare:30 |