| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:16017763-16018151 | Common:5; Rare:143 | ||||
| chr1:16352401-16352564 | Common:2; Rare:90 | ||||
| chr1:16613508-16613618 | |||||
| chr1:18902524-18902796 | Common:2; Rare:87; Clinvar:9 | ||||
| chr1:19210071-19210428 | Rare:129 | ||||
| chr1:19251510-19251866 | Common:6; Rare:116 | ||||
| chr1:19311982-19312371 | Common:8; Rare:175 | ||||
| chr1:19799872-19799987 | Common:1; Rare:43 | ||||
| chr1:20661346-20661703 | Common:3; Rare:128; Clinvar:4; Clinvar (benign):6 | ||||
| chr1:21176878-21177102 | Rare:54 | ||||
| chr1:21345476-21345674 | Common:1; Rare:75 | ||||
| chr1:23368297-23368513 | Common:1; Rare:54 | ||||
| chr1:23368854-23368974 | Common:1; Rare:42 | ||||
| chr1:23424563-23424898 | Common:1; Rare:93 | ||||
| chr1:23559413-23559648 | Common:1; Rare:101 |