| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:111757146-111757258 | Common:4; Rare:21 | ||||
| chr5:111757579-111757825 | Common:1; Rare:106 | ||||
| chr5:111757946-111758070 | Common:1; Rare:41 | ||||
| chr5:112737790-112737889 | Rare:23; Clinvar (benign):1 | ||||
| chr5:112861195-112861403 | Common:4; Rare:85 | ||||
| chr5:112976457-112976896 | Common:4; Rare:206 | ||||
| chr5:113513660-113513711 | Rare:14 | ||||
| chr5:115262827-115262931 | Rare:50 | ||||
| chr5:115816654-115816717 | Rare:13 | ||||
| chr5:115841548-115841619 | Common:1; Rare:41 | ||||
| chr5:115841818-115842016 | Common:3; Rare:65 | ||||
| chr5:116084715-116085055 | Common:9; Rare:113 | ||||
| chr5:119268590-119268811 | Common:1; Rare:64 | ||||
| chr5:119452380-119452555 | Common:1; Rare:61; Clinvar (benign):3 | ||||
| chr5:122774859-122775101 | Common:1; Rare:93 |