| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:16465715-16465895 | Rare:32 | ||||
| chr5:31532066-31532319 | Common:1; Rare:67 | ||||
| chr5:34915483-34915741 | Common:1; Rare:62 | ||||
| chr5:36151885-36152145 | Rare:74 | ||||
| chr5:37379273-37379335 | Rare:13 | ||||
| chr5:38845761-38846053 | Common:1; Rare:75 | ||||
| chr5:40798168-40798276 | Rare:49 | ||||
| chr5:40834590-40834670 | Common:1; Rare:20 | ||||
| chr5:43067434-43067476 | Rare:4 | ||||
| chr5:43603087-43603225 | Rare:35 | ||||
| chr5:53109722-53109860 | Rare:74; Clinvar:2 | ||||
| chr5:55307657-55308009 | Common:4; Rare:113 | ||||
| chr5:57173762-57174069 | Common:1; Rare:109 | ||||
| chr5:60945056-60945238 | Common:4; Rare:64; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:61162395-61162625 | Common:1; Rare:69 |