| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30617479-30618046 | Common:1; Rare:184 | ||||
| chr13:31162341-31162554 | Common:2; Rare:60 | ||||
| chr13:32031255-32031425 | Common:1; Rare:48 | ||||
| chr13:32031635-32031816 | Common:1; Rare:52 | ||||
| chr13:32315409-32315571 | Common:1; Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
| chr13:32315815-32315980 | Common:3; Rare:38; Clinvar (benign):3 | ||||
| chr13:32428128-32428369 | Rare:42 | ||||
| chr13:32538671-32538926 | Common:1; Rare:73 | ||||
| chr13:32586225-32586587 | Common:2; Rare:112 | ||||
| chr13:33285703-33285913 | Rare:49 | ||||
| chr13:33818007-33818365 | Common:1; Rare:153 | ||||
| chr13:34942156-34942314 | Common:3; Rare:46 | ||||
| chr13:35476295-35476882 | Common:2; Rare:104 | ||||
| chr13:36131145-36131486 | Common:1; Rare:82 | ||||
| chr13:36297783-36297909 | Rare:45 |