| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:33205992-33206124 | Rare:31 | ||||
| chr13:33285677-33285968 | Common:1; Rare:64 | ||||
| chr13:34942169-34942298 | Common:3; Rare:39 | ||||
| chr13:35476648-35476844 | Common:1; Rare:30 | ||||
| chr13:36346271-36346454 | Common:2; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:36346622-36346787 | Common:4; Rare:46 | ||||
| chr13:37000757-37000808 | Rare:25 | ||||
| chr13:37059596-37059765 | Common:1; Rare:58 | ||||
| chr13:38350229-38350284 | Rare:29 | ||||
| chr13:38686861-38687109 | Common:3; Rare:72; Clinvar:3; Clinvar (benign):1 | ||||
| chr13:39038021-39038460 | Common:1; Rare:110 | ||||
| chr13:39655619-39655802 | Common:2; Rare:91; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr13:40771121-40771328 | Common:3; Rare:66 | ||||
| chr13:41060880-41061043 | Common:16; Rare:98 | ||||
| chr13:41061395-41061645 | Common:2; Rare:73 |