| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139556369-139556567 | Rare:29 | ||||
| chr4:140373401-140373680 | Common:2; Rare:109 | ||||
| chr4:145098156-145098337 | Rare:65 | ||||
| chr4:147684154-147684346 | Rare:86 | ||||
| chr4:174283652-174283911 | Common:1; Rare:46 | ||||
| chr4:183659112-183659323 | Common:1; Rare:67 | ||||
| chr4:184649440-184649756 | Common:4; Rare:102 | ||||
| chr4:189940613-189940951 | Common:9; Rare:117 | ||||
| chr5:218134-218352 | Common:2; Rare:83; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:1799795-1799986 | Common:4; Rare:91 | ||||
| chr5:1801315-1801423 | Common:2; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:10249874-10250170 | Common:16; Rare:141 | ||||
| chr5:10353594-10353892 | Common:3; Rare:108 | ||||
| chr5:16465715-16466044 | Common:1; Rare:77 | ||||
| chr5:31532070-31532319 | Common:1; Rare:66 |