| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:36431964-36432559 | Common:6; Rare:399 | ||||
| chr13:36673760-36674140 | Common:1; Rare:114 | ||||
| chr13:36819056-36819242 | Common:1; Rare:74 | ||||
| chr13:36919810-36920420 | Common:13; Rare:224; Clinvar:6; Clinvar (benign):2 | ||||
| chr13:36999224-36999458 | Rare:102 | ||||
| chr13:37000058-37000415 | Common:2; Rare:77 | ||||
| chr13:37000485-37000854 | Common:3; Rare:123; Clinvar (pathogenic):1 | ||||
| chr13:37058755-37059155 | Rare:140 | ||||
| chr13:37059428-37059889 | Common:3; Rare:151 | ||||
| chr13:37869210-37869335 | Common:1; Rare:16 | ||||
| chr13:37869751-37869936 | Common:1; Rare:45 | ||||
| chr13:38349423-38349899 | Common:5; Rare:146; Clinvar (pathogenic):1 | ||||
| chr13:38686871-38687120 | Common:3; Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:39037797-39038416 | Common:2; Rare:178 | ||||
| chr13:39602622-39602727 | Rare:31 |