| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:95301355-95301526 | Common:1; Rare:50 | ||||
| chr13:95644367-95644528 | Common:1; Rare:44 | ||||
| chr13:95644545-95644815 | Common:1; Rare:65 | ||||
| chr13:95676916-95677220 | Common:3; Rare:109 | ||||
| chr13:96053327-96053515 | Common:2; Rare:87 | ||||
| chr13:97975621-97975972 | Common:3; Rare:98 | ||||
| chr13:97976372-97976782 | Common:1; Rare:149 | ||||
| chr13:98576744-98576968 | Common:3; Rare:59 | ||||
| chr13:98577063-98577255 | Common:1; Rare:58 | ||||
| chr13:99086635-99086741 | Rare:44 | ||||
| chr13:99200652-99200942 | Common:7; Rare:132 | ||||
| chr13:99981584-99981784 | Common:1; Rare:69 | ||||
| chr13:100088757-100089213 | Rare:172; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr13:100674754-100675061 | Common:3; Rare:125 | ||||
| chr13:100675067-100675171 | Common:1; Rare:43 |