| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:120066775-120066955 | Common:3; Rare:54 | ||||
| chr4:122152272-122152383 | Common:2; Rare:48 | ||||
| chr4:140373390-140373698 | Common:2; Rare:126 | ||||
| chr4:145098156-145098335 | Rare:64 | ||||
| chr4:152779796-152779993 | Common:1; Rare:51 | ||||
| chr4:158671849-158672132 | Common:4; Rare:74 | ||||
| chr4:165327400-165327692 | Common:2; Rare:83 | ||||
| chr4:177442410-177442555 | Rare:84; Clinvar:2 | ||||
| chr4:183659105-183659300 | Common:1; Rare:61 | ||||
| chr4:184649442-184649737 | Common:3; Rare:96 | ||||
| chr4:185425951-185426265 | Common:2; Rare:85 | ||||
| chr4:189940666-189940894 | Common:6; Rare:76 | ||||
| chr5:218125-218353 | Common:3; Rare:88; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:892743-892941 | Common:2; Rare:80 | ||||
| chr5:1801289-1801438 | Common:4; Rare:70; Clinvar:1; Clinvar (benign):1 |