| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183659083-183659395 | Common:1; Rare:100 | ||||
| chr4:184474519-184474816 | Rare:66 | ||||
| chr4:184649406-184649797 | Common:4; Rare:126 | ||||
| chr4:184734023-184734383 | Common:7; Rare:149 | ||||
| chr4:185143153-185143285 | Common:1; Rare:42; Clinvar (benign):2 | ||||
| chr4:185396561-185396850 | Rare:94 | ||||
| chr4:185425866-185426267 | Common:4; Rare:124 | ||||
| chr4:185535345-185535485 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:185535488-185535647 | Rare:43 | ||||
| chr4:189940588-189941004 | Common:16; Rare:140 | ||||
| chr5:218114-218358 | Common:3; Rare:98; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr5:443095-443260 | Common:7; Rare:74 | ||||
| chr5:892726-892923 | Common:3; Rare:75 | ||||
| chr5:1799791-1799993 | Common:4; Rare:94 | ||||
| chr5:1801300-1801455 | Common:4; Rare:78; Clinvar:3; Clinvar (benign):1 |