| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:35713094-35713856 | Common:9; Rare:285 | ||||
| chr13:36002830-36003230 | Common:1; Rare:72 | ||||
| chr13:36006030-36006790 | Common:2; Rare:229 | ||||
| chr13:36006961-36007225 | Common:2; Rare:59 | ||||
| chr13:36527970-36528400 | Common:7; Rare:84 | ||||
| chr13:37927001-37927401 | Common:5; Rare:123 | ||||
| chr13:37944100-37944420 | Common:3; Rare:52 | ||||
| chr13:38093006-38094139 | Common:8; Rare:301 | ||||
| chr13:38426789-38426967 | Common:1; Rare:41 | ||||
| chr13:38686329-38686542 | Common:3; Rare:77 | ||||
| chr13:38687960-38688360 | Common:1; Rare:181; Clinvar:7; Clinvar (benign):1 | ||||
| chr13:38735684-38735899 | Rare:40 | ||||
| chr13:38763208-38764279 | Common:7; Rare:282 | ||||
| chr13:39286410-39286810 | Common:14; Rare:128 | ||||
| chr13:39372770-39373328 | Common:9; Rare:192 |