| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:132675529-132675656 | Rare:36 | ||||
| chr8:133297132-133297525 | Common:3; Rare:153; Clinvar:4; Clinvar (benign):1 | ||||
| chr8:133571807-133572168 | Common:1; Rare:87 | ||||
| chr8:134713002-134713221 | Common:1; Rare:70 | ||||
| chr8:140511270-140511611 | Common:1; Rare:129 | ||||
| chr8:140718477-140718813 | Rare:61 | ||||
| chr8:141001136-141001496 | Common:4; Rare:126 | ||||
| chr8:141128275-141128701 | Common:5; Rare:131 | ||||
| chr8:142669940-142670329 | Common:9; Rare:134 | ||||
| chr8:142726984-142727291 | Common:4; Rare:113 | ||||
| chr8:143018393-143018558 | Common:2; Rare:50 | ||||
| chr8:143213046-143213255 | Rare:54 | ||||
| chr8:143267156-143267473 | Common:1; Rare:124 | ||||
| chr8:143291274-143291565 | Common:6; Rare:80 | ||||
| chr8:143310214-143310491 | Common:1; Rare:68 |