| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:154754990-154755343 | Common:4; Rare:108 | ||||
| chr5:154850532-154850722 | Common:1; Rare:35 | ||||
| chr5:154857758-154857890 | Rare:36 | ||||
| chr5:154857947-154858259 | Common:6; Rare:99 | ||||
| chr5:154858449-154858768 | Common:1; Rare:103 | ||||
| chr5:154938186-154938283 | Rare:29 | ||||
| chr5:154941034-154941123 | Common:1; Rare:42 | ||||
| chr5:157143637-157143905 | Rare:56 | ||||
| chr5:157266026-157266189 | Common:1; Rare:47 | ||||
| chr5:157791973-157792015 | Rare:18 | ||||
| chr5:157858951-157859264 | Common:2; Rare:98 | ||||
| chr5:159207908-159208218 | Common:3; Rare:65 | ||||
| chr5:159263191-159263337 | Common:1; Rare:46 | ||||
| chr5:160419049-160419261 | Common:4; Rare:80 | ||||
| chr5:161546696-161547065 | Common:1; Rare:68; Clinvar (benign):2 |