| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:20773139-20774251 | Common:14; Rare:1037 | ||||
| chr13:20901886-20902322 | Common:4; Rare:167 | ||||
| chr13:20902672-20903058 | Common:6; Rare:337 | ||||
| chr13:20902977-20903377 | Common:1; Rare:121 | ||||
| chr13:21022791-21023303 | Common:12; Rare:127 | ||||
| chr13:21061040-21061280 | Rare:68 | ||||
| chr13:21061467-21061867 | Common:4; Rare:299 | ||||
| chr13:21140249-21140720 | Rare:914 | ||||
| chr13:21176158-21176382 | Common:4; Rare:92 | ||||
| chr13:21176389-21176963 | Common:25; Rare:1031 | ||||
| chr13:21459160-21459651 | Common:9; Rare:407 | ||||
| chr13:21603601-21604074 | Rare:1038 | ||||
| chr13:21604080-21604350 | Common:21; Rare:507 | ||||
| chr13:21670197-21671239 | Common:6; Rare:380; Clinvar:2; Clinvar (benign):5 | ||||
| chr13:23374771-23375171 | Common:3; Rare:95; Clinvar:1; Clinvar (benign):2 |