| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185425866-185426263 | Common:4; Rare:122 | ||||
| chr4:186723783-186723936 | Common:4; Rare:58 | ||||
| chr4:189940593-189940964 | Common:11; Rare:124 | ||||
| chr5:218134-218379 | Common:3; Rare:105; Clinvar:9; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr5:612172-612351 | Rare:71 | ||||
| chr5:892716-892941 | Common:4; Rare:85 | ||||
| chr5:1799791-1799949 | Common:4; Rare:79 | ||||
| chr5:1801300-1801447 | Common:4; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:6378507-6378706 | Rare:74 | ||||
| chr5:7869000-7869194 | Common:2; Rare:96; Clinvar (benign):1 | ||||
| chr5:9545982-9546361 | Common:10; Rare:94 | ||||
| chr5:10249869-10250445 | Common:19; Rare:266; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10353597-10353898 | Common:3; Rare:110 | ||||
| chr5:16465715-16465875 | Rare:25 | ||||
| chr5:31532052-31532362 | Common:3; Rare:93 |