| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:186723666-186723918 | Common:5; Rare:96 | ||||
| chr4:188139317-188139460 | Common:1; Rare:24 | ||||
| chr4:189940547-189941012 | Common:16; Rare:153 | ||||
| chr5:218087-218415 | Common:4; Rare:129; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr5:322527-322661 | Rare:34 | ||||
| chr5:420728-420954 | Common:7; Rare:75 | ||||
| chr5:443069-443290 | Common:10; Rare:104 | ||||
| chr5:612172-612358 | Rare:74 | ||||
| chr5:891488-891577 | Rare:18 | ||||
| chr5:892489-892949 | Common:5; Rare:145 | ||||
| chr5:1064234-1064424 | Common:2; Rare:58 | ||||
| chr5:1111960-1112122 | Rare:62 | ||||
| chr5:1344830-1345217 | Common:2; Rare:126 | ||||
| chr5:1799778-1799996 | Common:8; Rare:104 | ||||
| chr5:1801287-1801460 | Common:4; Rare:87; Clinvar:3; Clinvar (benign):1 |