| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:102864159-102864475 | Common:2; Rare:118 | ||||
| chr8:103415094-103415449 | Common:6; Rare:182 | ||||
| chr8:108443437-108443653 | Common:4; Rare:92 | ||||
| chr8:109334078-109334402 | Common:1; Rare:80 | ||||
| chr8:118951883-118952133 | Common:1; Rare:65; Clinvar:7; Clinvar (benign):1 | ||||
| chr8:120445103-120445185 | Common:1; Rare:21 | ||||
| chr8:124539040-124539198 | Common:2; Rare:89; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:125091748-125091892 | Common:1; Rare:47 | ||||
| chr9:4679487-4679701 | Rare:95 | ||||
| chr9:18474003-18474172 | Rare:40 | ||||
| chr9:19380184-19380377 | Common:5; Rare:91 | ||||
| chr9:33025098-33025304 | Common:5; Rare:86 | ||||
| chr9:33076620-33076850 | Common:2; Rare:78 | ||||
| chr9:33290363-33290565 | Common:2; Rare:76 | ||||
| chr9:35657996-35658318 | Common:5; Rare:245; Clinvar:18; Clinvar (benign):10; Clinvar (pathogenic):33 |