| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144103713-144103896 | Rare:60 | ||||
| chr8:144104153-144104550 | Common:3; Rare:139 | ||||
| chr8:144104752-144104839 | Common:1; Rare:25 | ||||
| chr8:144291357-144291668 | Common:1; Rare:100 | ||||
| chr8:144326850-144327043 | Common:1; Rare:52 | ||||
| chr8:144502894-144503073 | Common:2; Rare:43 | ||||
| chr8:144503996-144504149 | Rare:32 | ||||
| chr8:144508950-144509106 | Rare:44 | ||||
| chr8:144755461-144755691 | Common:1; Rare:76 | ||||
| chr8:144792318-144792562 | Common:3; Rare:92 | ||||
| chr8:144827241-144827603 | Common:2; Rare:93 | ||||
| chr8:144852998-144853154 | Rare:55 | ||||
| chr8:144901416-144901699 | Common:1; Rare:82 | ||||
| chr9:2017492-2017725 | Rare:71 | ||||
| chr9:2621842-2622192 | Common:6; Rare:126; Clinvar:9; Clinvar (benign):3 |