| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48037604-48037866 | Common:2; Rare:117; Clinvar:2 | ||||
| chr13:48037924-48038141 | Common:5; Rare:64 | ||||
| chr13:48233129-48233473 | Common:2; Rare:121 | ||||
| chr13:48303657-48303857 | Rare:65; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48975887-48975928 | Rare:8 | ||||
| chr13:49110217-49110376 | Common:2; Rare:50 | ||||
| chr13:49247812-49248083 | Rare:79 | ||||
| chr13:49443955-49444437 | Common:1; Rare:150 | ||||
| chr13:49495902-49496009 | Rare:18 | ||||
| chr13:49585471-49585644 | Common:1; Rare:59 | ||||
| chr13:49628265-49628496 | Common:1; Rare:50 | ||||
| chr13:49691255-49691528 | Common:2; Rare:101 | ||||
| chr13:49706158-49706352 | Rare:47 | ||||
| chr13:49793030-49793190 | Common:3; Rare:54 | ||||
| chr13:49936236-49936575 | Common:1; Rare:103 |