| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:126809845-126810245 | Common:3; Rare:119 | ||||
| chr8:127736886-127737632 | Common:3; Rare:210 | ||||
| chr8:127738119-127738519 | Common:8; Rare:204; Clinvar (pathogenic):10 | ||||
| chr8:127794280-127794640 | Rare:90 | ||||
| chr8:127795604-127795844 | Common:1; Rare:34 | ||||
| chr8:127809584-127810073 | Common:5; Rare:190 | ||||
| chr8:127810115-127810515 | Common:1; Rare:139 | ||||
| chr8:128313736-128314136 | Common:5; Rare:171 | ||||
| chr8:128874336-128874942 | Common:9; Rare:191 | ||||
| chr8:128935692-128936523 | Common:5; Rare:236 | ||||
| chr8:129077701-129078203 | Common:2; Rare:125 | ||||
| chr8:129260620-129260940 | Common:1; Rare:65 | ||||
| chr8:130302461-130302861 | Common:3; Rare:102 | ||||
| chr8:130357478-130358257 | Common:3; Rare:366 | ||||
| chr8:130358569-130358814 | Common:1; Rare:108 |