| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:108748732-108748993 | Common:1; Rare:86 | ||||
| chr5:109408915-109409117 | Common:4; Rare:52 | ||||
| chr5:109409858-109410018 | Common:4; Rare:75 | ||||
| chr5:109689287-109689440 | Common:4; Rare:80 | ||||
| chr5:110738913-110739061 | Common:1; Rare:49 | ||||
| chr5:115841534-115841625 | Common:1; Rare:55 | ||||
| chr5:115841799-115842024 | Common:3; Rare:74 | ||||
| chr5:116084727-116085055 | Common:8; Rare:111 | ||||
| chr5:119268625-119268811 | Common:1; Rare:55 | ||||
| chr5:119355819-119355959 | Common:1; Rare:43 | ||||
| chr5:122845503-122845639 | Common:3; Rare:53 | ||||
| chr5:124748760-124748997 | Common:2; Rare:54 | ||||
| chr5:127290654-127290873 | Rare:44 | ||||
| chr5:128083058-128083390 | Common:8; Rare:103 | ||||
| chr5:131170693-131171008 | Common:1; Rare:67; Clinvar (benign):2 |