| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:109272544-109272582 | Rare:8 | ||||
| chr13:109273719-109273750 | Rare:3 | ||||
| chr13:110424825-110424965 | Common:4; Rare:49; Clinvar:3; Clinvar (benign):2 | ||||
| chr13:110503195-110503398 | Common:1; Rare:59; Clinvar:1 | ||||
| chr13:110609888-110610001 | Rare:16 | ||||
| chr13:110724243-110724287 | Rare:8 | ||||
| chr13:110892118-110892411 | Common:1; Rare:52 | ||||
| chr13:110896992-110897144 | Common:3; Rare:39 | ||||
| chr13:110897147-110897407 | Common:2; Rare:59 | ||||
| chr13:110898201-110898352 | Common:1; Rare:23 | ||||
| chr13:110899930-110900095 | Common:2; Rare:30 | ||||
| chr13:110903385-110903938 | Common:1; Rare:113 | ||||
| chr13:111211270-111211394 | Common:1; Rare:18 | ||||
| chr13:111280326-111280643 | Common:2; Rare:94 | ||||
| chr13:112091296-112091409 | Rare:7 |