| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:32031611-32031669 | Rare:13 | ||||
| chr13:32031678-32031816 | Common:1; Rare:44 | ||||
| chr13:32315400-32315561 | Common:1; Rare:48; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:32586248-32586582 | Common:2; Rare:101 | ||||
| chr13:33206022-33206146 | Rare:25 | ||||
| chr13:33285710-33285880 | Rare:38 | ||||
| chr13:33818045-33818204 | Rare:74 | ||||
| chr13:34942165-34942353 | Common:3; Rare:64 | ||||
| chr13:35476314-35476854 | Common:1; Rare:96 | ||||
| chr13:35855587-35855752 | Common:1; Rare:37 | ||||
| chr13:36131156-36131541 | Common:1; Rare:96 | ||||
| chr13:36297787-36297893 | Rare:35 | ||||
| chr13:36346271-36346485 | Common:3; Rare:60; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:36999265-36999448 | Rare:73 | ||||
| chr13:37000518-37000805 | Common:3; Rare:90 |