| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:80407836-80408121 | Common:2; Rare:197 | ||||
| chr5:80487868-80488126 | Common:2; Rare:154 | ||||
| chr5:80654559-80654746 | Common:5; Rare:117 | ||||
| chr5:80654883-80655201 | Common:24; Rare:278; Clinvar:2; Clinvar (benign):6 | ||||
| chr5:81301461-81301877 | Common:11; Rare:191 | ||||
| chr5:81751002-81751522 | Common:2; Rare:242 | ||||
| chr5:81971749-81972503 | Common:9; Rare:363 | ||||
| chr5:82278310-82278730 | Common:8; Rare:270 | ||||
| chr5:83077320-83077627 | Common:2; Rare:188 | ||||
| chr5:86617768-86618103 | Common:4; Rare:192 | ||||
| chr5:87267690-87268065 | Common:8; Rare:236 | ||||
| chr5:87268060-87268500 | Common:4; Rare:181; Clinvar:3; Clinvar (benign):4 | ||||
| chr5:87268821-87268946 | Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:87412160-87412550 | Rare:102 | ||||
| chr5:87412795-87413136 | Common:8; Rare:213 |