| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:40771129-40771430 | Common:3; Rare:91 | ||||
| chr13:40789347-40789615 | Common:2; Rare:90; Clinvar:5; Clinvar (benign):2 | ||||
| chr13:41061156-41061654 | Common:4; Rare:170 | ||||
| chr13:41132715-41132971 | Rare:67 | ||||
| chr13:41263535-41263592 | Rare:14 | ||||
| chr13:43023501-43023657 | Common:1; Rare:60 | ||||
| chr13:43786862-43786961 | Rare:30 | ||||
| chr13:43879705-43879904 | Common:18; Rare:60 | ||||
| chr13:44436829-44436997 | Common:2; Rare:52 | ||||
| chr13:44989461-44989603 | Rare:51 | ||||
| chr13:45120177-45120602 | Common:2; Rare:105 | ||||
| chr13:45341040-45341525 | Common:4; Rare:233 | ||||
| chr13:45418436-45418578 | Rare:39 | ||||
| chr13:46052718-46052899 | Common:2; Rare:55 | ||||
| chr13:46797117-46797337 | Common:3; Rare:77 |