| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:112588045-112588346 | Rare:81 | ||||
| chr13:112588520-112588911 | Common:3; Rare:85 | ||||
| chr13:112689724-112690279 | Common:6; Rare:161 | ||||
| chr13:112690364-112690494 | Common:1; Rare:38 | ||||
| chr13:112690525-112690662 | Rare:20 | ||||
| chr13:112893618-112893878 | Common:3; Rare:48 | ||||
| chr13:112893961-112894533 | Common:16; Rare:199 | ||||
| chr13:112968690-112968773 | Rare:24 | ||||
| chr13:112969018-112969316 | Common:2; Rare:78 | ||||
| chr13:112969398-112969461 | Rare:10 | ||||
| chr13:113001533-113001740 | Common:1; Rare:44 | ||||
| chr13:113002275-113002449 | Common:2; Rare:29 | ||||
| chr13:113105339-113106223 | Common:10; Rare:216; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr13:113122606-113122901 | Common:3; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:113158531-113158666 | Common:2; Rare:44 |