| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143986398-143986502 | Rare:18 | ||||
| chr8:143992477-143992833 | Common:2; Rare:117 | ||||
| chr8:144060684-144060820 | Rare:40 | ||||
| chr8:144078477-144078722 | Common:1; Rare:75 | ||||
| chr8:144082513-144082709 | Common:2; Rare:65 | ||||
| chr8:144096076-144096419 | Common:1; Rare:134; Clinvar (benign):3 | ||||
| chr8:144103638-144103872 | Common:1; Rare:81 | ||||
| chr8:144104159-144104516 | Common:3; Rare:117 | ||||
| chr8:144104752-144104844 | Common:1; Rare:26 | ||||
| chr8:144147837-144148058 | Common:1; Rare:53 | ||||
| chr8:144291372-144291660 | Common:1; Rare:96 | ||||
| chr8:144413526-144413723 | Common:1; Rare:62; Clinvar:1 | ||||
| chr8:144428489-144428863 | Common:9; Rare:148 | ||||
| chr8:144462861-144463049 | Rare:88 | ||||
| chr8:144465355-144465423 | Rare:25 |