| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183659105-183659446 | Common:1; Rare:109 | ||||
| chr4:184474484-184474816 | Rare:72 | ||||
| chr4:184649396-184649812 | Common:5; Rare:136 | ||||
| chr4:185425877-185426252 | Common:3; Rare:110 | ||||
| chr4:186726655-186726959 | Common:4; Rare:102 | ||||
| chr4:189940657-189940967 | Common:9; Rare:110 | ||||
| chr5:218123-218385 | Common:3; Rare:113; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr5:443084-443263 | Common:9; Rare:81 | ||||
| chr5:892541-892941 | Common:5; Rare:124 | ||||
| chr5:1799785-1799961 | Common:7; Rare:87 | ||||
| chr5:1801300-1801455 | Common:4; Rare:78; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:6378480-6378706 | Rare:95 | ||||
| chr5:6632967-6633313 | Common:6; Rare:107; Clinvar:8; Clinvar (benign):3 | ||||
| chr5:7869000-7869194 | Common:2; Rare:96; Clinvar (benign):1 | ||||
| chr5:10249869-10250183 | Common:16; Rare:144 |