| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:110738914-110739112 | Common:2; Rare:81 | ||||
| chr5:111092286-111092420 | Common:2; Rare:75; Clinvar (benign):4 | ||||
| chr5:111512418-111512750 | Common:3; Rare:116 | ||||
| chr5:112419131-112419401 | Common:4; Rare:101 | ||||
| chr5:112976478-112976907 | Common:3; Rare:207 | ||||
| chr5:113294629-113294720 | Rare:24 | ||||
| chr5:115262829-115262898 | Rare:34 | ||||
| chr5:115544639-115545014 | Common:2; Rare:139 | ||||
| chr5:115602410-115602492 | Rare:23 | ||||
| chr5:115626005-115626247 | Rare:71 | ||||
| chr5:115816281-115816393 | Common:1; Rare:41 | ||||
| chr5:115816398-115816581 | Common:1; Rare:54 | ||||
| chr5:115816859-115817038 | Common:1; Rare:42 | ||||
| chr5:115841505-115841642 | Common:3; Rare:83 | ||||
| chr5:115841799-115842105 | Common:4; Rare:97 |