| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:37059593-37059883 | Common:3; Rare:109 | ||||
| chr13:37869744-37869892 | Common:1; Rare:36 | ||||
| chr13:38686890-38687105 | Common:3; Rare:59; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:39038087-39038433 | Common:1; Rare:87 | ||||
| chr13:39655627-39655740 | Common:1; Rare:66; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr13:40771078-40771262 | Common:1; Rare:75 | ||||
| chr13:41061356-41061570 | Common:2; Rare:64 | ||||
| chr13:41132777-41133008 | Rare:57 | ||||
| chr13:43879498-43879862 | Common:19; Rare:105 | ||||
| chr13:44435170-44435447 | Common:3; Rare:79 | ||||
| chr13:44436760-44436988 | Common:2; Rare:68 | ||||
| chr13:44989428-44989616 | Rare:71 | ||||
| chr13:45120392-45120648 | Common:1; Rare:86 | ||||
| chr13:45341040-45341609 | Common:4; Rare:258 | ||||
| chr13:46052692-46052835 | Common:2; Rare:41 |