| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:40755884-40756111 | Rare:62 | ||||
| chr5:40798130-40798448 | Common:1; Rare:125 | ||||
| chr5:40834219-40834655 | Common:4; Rare:127 | ||||
| chr5:40834954-40835406 | Common:3; Rare:173 | ||||
| chr5:40841305-40841383 | Rare:22 | ||||
| chr5:40841584-40841653 | Common:1; Rare:22 | ||||
| chr5:41870360-41870672 | Common:2; Rare:97; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:41903955-41904421 | Common:2; Rare:152 | ||||
| chr5:41925151-41925238 | Common:1; Rare:39 | ||||
| chr5:41925241-41925316 | Rare:21 | ||||
| chr5:42423354-42423505 | Common:2; Rare:32 | ||||
| chr5:42423579-42423935 | Common:2; Rare:96; Clinvar (benign):1 | ||||
| chr5:42424889-42425004 | Rare:24 | ||||
| chr5:43043168-43043326 | Common:1; Rare:30 | ||||
| chr5:43064815-43065174 | Common:1; Rare:84 |