| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:186724031-186724348 | Common:2; Rare:71 | ||||
| chr4:186726631-186726783 | Common:4; Rare:50 | ||||
| chr4:187995588-187995855 | Common:1; Rare:68 | ||||
| chr4:188109257-188109396 | Rare:24 | ||||
| chr4:188109400-188109442 | Rare:9 | ||||
| chr4:189940631-189941028 | Common:16; Rare:149 | ||||
| chr5:218109-218396 | Common:4; Rare:119; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr5:443074-443272 | Common:10; Rare:88 | ||||
| chr5:612190-612357 | Rare:67 | ||||
| chr5:892416-892999 | Common:5; Rare:185 | ||||
| chr5:1112006-1112114 | Rare:45 | ||||
| chr5:1295051-1295179 | Rare:35 | ||||
| chr5:1344945-1345217 | Common:1; Rare:98 | ||||
| chr5:1445415-1445570 | Common:1; Rare:41 | ||||
| chr5:1523715-1524065 | Common:1; Rare:97 |