| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:111092199-111092420 | Common:2; Rare:113; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:111482366-111482529 | Rare:28 | ||||
| chr5:111512412-111512720 | Common:3; Rare:110 | ||||
| chr5:112419142-112419491 | Common:5; Rare:121 | ||||
| chr5:112861156-112861427 | Common:5; Rare:107 | ||||
| chr5:112862190-112862396 | Common:5; Rare:48 | ||||
| chr5:112922186-112922370 | Common:1; Rare:91 | ||||
| chr5:112976544-112976847 | Common:2; Rare:135 | ||||
| chr5:113434945-113435083 | Rare:15 | ||||
| chr5:113488073-113488366 | Common:5; Rare:135 | ||||
| chr5:113513624-113513725 | Rare:33 | ||||
| chr5:115153779-115153898 | Rare:28 | ||||
| chr5:115169646-115170009 | Rare:128 | ||||
| chr5:115180202-115180400 | Common:2; Rare:61 | ||||
| chr5:115262804-115262921 | Common:1; Rare:56 |