| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:113854380-113854878 | Common:1; Rare:112 | ||||
| chr10:116545694-116546138 | Common:2; Rare:107 | ||||
| chr10:116590939-116591191 | Common:1; Rare:67 | ||||
| chr10:116597815-116598175 | Common:3; Rare:116 | ||||
| chr10:116849640-116849822 | Rare:63 | ||||
| chr10:117005087-117005443 | Common:2; Rare:104 | ||||
| chr10:118046678-118047013 | Common:4; Rare:107 | ||||
| chr10:119080757-119080929 | Rare:68 | ||||
| chr10:119178756-119178936 | Common:3; Rare:77 | ||||
| chr10:119892536-119892777 | Common:3; Rare:91 | ||||
| chr10:120851200-120851411 | Common:4; Rare:73 | ||||
| chr10:121927930-121928076 | Common:1; Rare:58 | ||||
| chr10:121928459-121928500 | Rare:10 | ||||
| chr10:122954197-122954486 | Rare:107 | ||||
| chr10:123008788-123009023 | Common:5; Rare:63; Clinvar:4; Clinvar (benign):5 |