| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:56233283-56233429 | Rare:28 | ||||
| chr5:56952100-56952304 | Rare:74 | ||||
| chr5:57173740-57174165 | Common:1; Rare:150 | ||||
| chr5:58459964-58460242 | Common:6; Rare:115 | ||||
| chr5:58582028-58582322 | Common:1; Rare:53 | ||||
| chr5:58582326-58582407 | Rare:15 | ||||
| chr5:58582903-58583243 | Common:2; Rare:86 | ||||
| chr5:58788176-58788347 | Common:1; Rare:30 | ||||
| chr5:58999841-59000120 | Rare:55 | ||||
| chr5:59893295-59893624 | Rare:103; Clinvar (benign):1 | ||||
| chr5:60700074-60700246 | Common:1; Rare:69 | ||||
| chr5:60945022-60945258 | Common:5; Rare:90; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr5:61162236-61162499 | Common:1; Rare:55 | ||||
| chr5:62403821-62404042 | Common:3; Rare:76 | ||||
| chr5:62412545-62412788 | Rare:77 |