| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183659736-183660166 | Common:2; Rare:150 | ||||
| chr4:184473163-184473885 | Common:4; Rare:242 | ||||
| chr4:184473904-184474304 | Common:7; Rare:138 | ||||
| chr4:184474452-184475317 | Common:6; Rare:643 | ||||
| chr4:184649377-184649864 | Common:33; Rare:936 | ||||
| chr4:184650132-184650433 | Common:2; Rare:66 | ||||
| chr4:184733231-184733631 | Common:19; Rare:290 | ||||
| chr4:184733942-184734525 | Common:44; Rare:910 | ||||
| chr4:184825220-184826390 | Common:36; Rare:803 | ||||
| chr4:185142910-185143340 | Common:19; Rare:463; Clinvar:1; Clinvar (benign):16 | ||||
| chr4:185203281-185203828 | Common:9; Rare:197 | ||||
| chr4:185203835-185204821 | Common:14; Rare:469 | ||||
| chr4:185209296-185210548 | Common:22; Rare:1362 | ||||
| chr4:185395670-185396901 | Common:14; Rare:1775 | ||||
| chr4:185425708-185426278 | Common:21; Rare:642 |