| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:184649399-184649805 | Common:4; Rare:133 | ||||
| chr4:184734044-184734426 | Common:6; Rare:142 | ||||
| chr4:184805461-184805832 | Common:1; Rare:69 | ||||
| chr4:184825931-184826311 | Common:7; Rare:110 | ||||
| chr4:185143129-185143310 | Common:2; Rare:59; Clinvar (benign):3 | ||||
| chr4:185203878-185204198 | Common:2; Rare:103 | ||||
| chr4:185396563-185396845 | Rare:92 | ||||
| chr4:185425872-185426265 | Common:4; Rare:120 | ||||
| chr4:185775802-185776025 | Common:1; Rare:34 | ||||
| chr4:185810985-185811140 | Common:1; Rare:37 | ||||
| chr4:185811961-185812281 | Common:1; Rare:58 | ||||
| chr4:185813098-185813333 | Common:2; Rare:34 | ||||
| chr4:186191472-186191942 | Common:8; Rare:147; Clinvar:3; Clinvar (benign):6 | ||||
| chr4:186250828-186251031 | Common:1; Rare:34 | ||||
| chr4:186265742-186266275 | Common:3; Rare:101; Clinvar:3; Clinvar (benign):2 |