| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:70203026-70203195 | Common:3; Rare:59 | ||||
| chr11:70203197-70203582 | Common:3; Rare:143; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:70203609-70204098 | Rare:127; Clinvar:1 | ||||
| chr11:70270405-70270808 | Common:2; Rare:159 | ||||
| chr11:70271051-70271198 | Rare:44 | ||||
| chr11:70398052-70398213 | Common:1; Rare:28 | ||||
| chr11:70398236-70398637 | Common:4; Rare:138 | ||||
| chr11:70398690-70398808 | Rare:18 | ||||
| chr11:71448323-71448690 | Common:4; Rare:98; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71452965-71453294 | Common:4; Rare:92 | ||||
| chr11:71453348-71453449 | Common:1; Rare:36 | ||||
| chr11:71453564-71453587 | Rare:4 | ||||
| chr11:71786763-71787122 | Common:2; Rare:103 | ||||
| chr11:71787303-71787695 | Common:19; Rare:175 | ||||
| chr11:71787715-71787841 | Common:1; Rare:45 |