| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:49997419-49997524 | Rare:34 | ||||
| chr13:50081943-50082312 | Common:1; Rare:105 | ||||
| chr13:50909691-50910358 | Common:3; Rare:160; Clinvar:6; Clinvar (benign):1 | ||||
| chr13:51222286-51222475 | Common:2; Rare:63 | ||||
| chr13:51452250-51452407 | Rare:47 | ||||
| chr13:51453013-51453412 | Common:1; Rare:153 | ||||
| chr13:51803576-51803836 | Rare:60 | ||||
| chr13:51804103-51804244 | Common:2; Rare:44 | ||||
| chr13:52012110-52012448 | Common:2; Rare:123; Clinvar:1 | ||||
| chr13:52455387-52455611 | Common:2; Rare:91 | ||||
| chr13:52455927-52456023 | Common:1; Rare:32 | ||||
| chr13:52652267-52652466 | Common:3; Rare:57 | ||||
| chr13:52652644-52653206 | Common:4; Rare:194 | ||||
| chr13:52739357-52739554 | Common:2; Rare:32 | ||||
| chr13:52739557-52740166 | Common:1; Rare:168 |