| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:34045382-34045791 | Common:4; Rare:125 | ||||
| chr13:34740248-34740469 | Rare:40 | ||||
| chr13:34750280-34750620 | Rare:77 | ||||
| chr13:35729876-35730551 | Common:3; Rare:180 | ||||
| chr13:36778063-36778597 | Common:12; Rare:247 | ||||
| chr13:36787065-36787465 | Common:3; Rare:97 | ||||
| chr13:38415366-38415530 | Rare:35 | ||||
| chr13:38419437-38419837 | Common:4; Rare:108 | ||||
| chr13:38824380-38824785 | Common:6; Rare:131 | ||||
| chr13:38850992-38851431 | Common:1; Rare:156; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr13:39036230-39036550 | Rare:97 | ||||
| chr13:39259370-39259790 | Common:9; Rare:86 | ||||
| chr13:39282530-39282930 | Common:8; Rare:109 | ||||
| chr13:39307310-39307670 | Common:2; Rare:58 | ||||
| chr13:39776520-39777055 | Common:4; Rare:143 |