| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183659112-183659349 | Common:1; Rare:77 | ||||
| chr4:184649439-184649783 | Common:4; Rare:110 | ||||
| chr4:184826026-184826175 | Common:4; Rare:51 | ||||
| chr4:185396581-185396843 | Rare:83 | ||||
| chr4:185425964-185426267 | Common:2; Rare:79 | ||||
| chr4:186723802-186724020 | Common:6; Rare:74 | ||||
| chr4:189940644-189940974 | Common:10; Rare:122 | ||||
| chr5:218093-218361 | Common:4; Rare:107; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr5:443079-443275 | Common:10; Rare:90 | ||||
| chr5:892520-892941 | Common:5; Rare:130 | ||||
| chr5:1799791-1799986 | Common:4; Rare:91 | ||||
| chr5:1801300-1801460 | Common:4; Rare:80; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:6632996-6633386 | Common:8; Rare:126; Clinvar:9; Clinvar (benign):4 | ||||
| chr5:7868987-7869204 | Common:2; Rare:112; Clinvar (benign):1 | ||||
| chr5:10249866-10250170 | Common:16; Rare:144 |