| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:111092233-111092432 | Common:2; Rare:107; Clinvar:1; Clinvar (benign):4 | ||||
| chr5:111224143-111224531 | Rare:152 | ||||
| chr5:111512445-111512751 | Common:3; Rare:109 | ||||
| chr5:111757152-111757335 | Common:5; Rare:37 | ||||
| chr5:111757378-111757845 | Common:1; Rare:173 | ||||
| chr5:112707368-112707661 | Common:8; Rare:129; Clinvar:69; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr5:112737623-112737767 | Rare:35; Clinvar (benign):2 | ||||
| chr5:112737797-112737923 | Rare:27; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:112921548-112921822 | Common:4; Rare:79 | ||||
| chr5:112976472-112976865 | Common:2; Rare:182 | ||||
| chr5:113203220-113203575 | Common:6; Rare:95 | ||||
| chr5:114363443-114363472 | Rare:8 | ||||
| chr5:115262823-115262936 | Common:1; Rare:53 | ||||
| chr5:115544648-115545024 | Common:2; Rare:141 | ||||
| chr5:115841490-115842081 | Common:8; Rare:254 |