| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:121928681-121928803 | Common:1; Rare:30 | ||||
| chr10:121928911-121928931 | Common:1; Rare:5 | ||||
| chr10:121974499-121974672 | Common:2; Rare:36 | ||||
| chr10:121974690-121974981 | Common:2; Rare:85 | ||||
| chr10:121975099-121975316 | Common:1; Rare:50 | ||||
| chr10:121975524-121975599 | Common:1; Rare:13 | ||||
| chr10:122019469-122019745 | Common:5; Rare:46 | ||||
| chr10:122112603-122113251 | Common:8; Rare:177 | ||||
| chr10:122113286-122113490 | Rare:36 | ||||
| chr10:122374406-122374853 | Common:3; Rare:137 | ||||
| chr10:122374861-122375337 | Common:2; Rare:165 | ||||
| chr10:122461356-122461665 | Common:1; Rare:90; Clinvar (benign):1 | ||||
| chr10:122461739-122462150 | Common:2; Rare:113; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr10:122879113-122879196 | Common:2; Rare:19 | ||||
| chr10:122879438-122879919 | Common:4; Rare:116 |