| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:33285653-33285934 | Common:1; Rare:64 | ||||
| chr13:34942156-34942306 | Common:3; Rare:44 | ||||
| chr13:35476672-35476809 | Common:1; Rare:19 | ||||
| chr13:36297794-36297923 | Rare:49 | ||||
| chr13:36346258-36346505 | Common:3; Rare:69; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:36673847-36674054 | Common:1; Rare:69 | ||||
| chr13:36999275-36999440 | Rare:68 | ||||
| chr13:37000246-37000400 | Common:2; Rare:29 | ||||
| chr13:37000561-37000805 | Common:2; Rare:80 | ||||
| chr13:37059449-37059757 | Common:1; Rare:88 | ||||
| chr13:38349548-38349932 | Common:3; Rare:133; Clinvar (pathogenic):1 | ||||
| chr13:38350208-38350310 | Rare:46 | ||||
| chr13:39038078-39038463 | Common:1; Rare:93 | ||||
| chr13:39603099-39603272 | Common:1; Rare:61 | ||||
| chr13:39655562-39655802 | Common:4; Rare:121; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 |