| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:46797103-46797337 | Common:3; Rare:79 | ||||
| chr13:48303674-48303894 | Rare:73; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48533050-48533140 | Common:1; Rare:30 | ||||
| chr13:48975753-48975923 | Common:2; Rare:55 | ||||
| chr13:48976478-48976656 | Common:2; Rare:61 | ||||
| chr13:49247830-49247976 | Rare:45 | ||||
| chr13:49444005-49444476 | Common:1; Rare:152 | ||||
| chr13:49495890-49496063 | Rare:39 | ||||
| chr13:49585520-49585617 | Common:1; Rare:32 | ||||
| chr13:49936211-49936543 | Common:1; Rare:107 | ||||
| chr13:49996827-49997088 | Common:1; Rare:41 | ||||
| chr13:50081980-50082262 | Common:1; Rare:78 | ||||
| chr13:51804121-51804219 | Common:2; Rare:30 | ||||
| chr13:52012084-52012421 | Common:2; Rare:108; Clinvar:1 | ||||
| chr13:52455344-52455548 | Common:3; Rare:77 |