| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:48094987-48095272 | Common:2; Rare:136 | ||||
| chr13:48233041-48233275 | Common:3; Rare:80 | ||||
| chr13:48303570-48304061 | Common:1; Rare:151; Clinvar:16; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr13:48492230-48492821 | Common:3; Rare:111 | ||||
| chr13:48532463-48532969 | Common:6; Rare:164 | ||||
| chr13:48532971-48533208 | Common:2; Rare:77 | ||||
| chr13:49247715-49248011 | Common:1; Rare:71 | ||||
| chr13:49443461-49443597 | Rare:18 | ||||
| chr13:49443881-49444593 | Common:3; Rare:219 | ||||
| chr13:49444649-49444753 | Common:5; Rare:21 | ||||
| chr13:49444756-49444905 | Rare:23 | ||||
| chr13:49445106-49445206 | Common:1; Rare:22 | ||||
| chr13:49445240-49445333 | Rare:15 | ||||
| chr13:49495546-49495620 | Rare:13 | ||||
| chr13:49495797-49496063 | Rare:65 |