| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:156970889-156971219 | Rare:56 | ||||
| chr4:156971767-156971945 | Common:1; Rare:66 | ||||
| chr4:158172360-158172734 | Rare:61 | ||||
| chr4:158172986-158173027 | Rare:8 | ||||
| chr4:158210311-158210559 | Common:2; Rare:56 | ||||
| chr4:158671859-158672365 | Common:5; Rare:120; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:163166826-163166954 | Common:2; Rare:41 | ||||
| chr4:163343612-163343942 | Common:3; Rare:87 | ||||
| chr4:163344330-163344436 | Common:2; Rare:16 | ||||
| chr4:165112810-165113022 | Common:1; Rare:62 | ||||
| chr4:165327412-165327734 | Common:2; Rare:93 | ||||
| chr4:168898397-168898606 | Common:1; Rare:64; Clinvar:8 | ||||
| chr4:169010236-169010497 | Common:1; Rare:80 | ||||
| chr4:169620391-169620725 | Common:2; Rare:115 | ||||
| chr4:169757866-169758074 | Rare:59 |