| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:30306813-30307236 | Common:7; Rare:123 | ||||
| chr13:30307330-30307621 | Common:3; Rare:86 | ||||
| chr13:30617233-30618056 | Common:1; Rare:248 | ||||
| chr13:31161716-31161800 | Common:1; Rare:38 | ||||
| chr13:31162300-31162461 | Common:1; Rare:49 | ||||
| chr13:32031089-32031223 | Common:1; Rare:22 | ||||
| chr13:32031258-32031521 | Common:1; Rare:67 | ||||
| chr13:32031539-32031817 | Common:1; Rare:73 | ||||
| chr13:32315379-32315542 | Common:1; Rare:48; Clinvar:2; Clinvar (benign):1 | ||||
| chr13:32586225-32586597 | Common:2; Rare:115 | ||||
| chr13:33818013-33818197 | Common:1; Rare:79 | ||||
| chr13:34942161-34942314 | Common:3; Rare:46 | ||||
| chr13:35476657-35476844 | Common:1; Rare:27 | ||||
| chr13:35855634-35855779 | Rare:28 | ||||
| chr13:36131117-36131561 | Common:1; Rare:107 |