| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30932613-30932708 | Rare:25 | ||||
| chr13:31162345-31162478 | Common:1; Rare:40 | ||||
| chr13:32031035-32031352 | Common:2; Rare:76 | ||||
| chr13:32315424-32315536 | Rare:33; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:32586250-32586593 | Common:2; Rare:106 | ||||
| chr13:33818015-33818171 | Common:1; Rare:64 | ||||
| chr13:34942156-34942306 | Common:3; Rare:44 | ||||
| chr13:35476687-35476822 | Common:1; Rare:21 | ||||
| chr13:35855543-35855751 | Common:1; Rare:47 | ||||
| chr13:36297787-36297897 | Rare:38 | ||||
| chr13:36346301-36346459 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36346687-36346781 | Common:3; Rare:33 | ||||
| chr13:37059596-37059737 | Common:1; Rare:48 | ||||
| chr13:37869725-37869882 | Common:1; Rare:39 | ||||
| chr13:38349533-38349932 | Common:4; Rare:136; Clinvar (pathogenic):1 |