| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:98928630-98928658 | Rare:7 | ||||
| chr5:98928849-98929206 | Common:4; Rare:146 | ||||
| chr5:100535215-100535635 | Rare:117 | ||||
| chr5:100903207-100903410 | Common:1; Rare:40 | ||||
| chr5:102296264-102296657 | Common:2; Rare:104 | ||||
| chr5:103120083-103120478 | Common:1; Rare:101 | ||||
| chr5:103258477-103258811 | Common:1; Rare:110 | ||||
| chr5:108748719-108748993 | Common:1; Rare:91 | ||||
| chr5:109409286-109409552 | Common:2; Rare:83 | ||||
| chr5:109409841-109410018 | Common:4; Rare:76 | ||||
| chr5:109689165-109689443 | Common:5; Rare:120 | ||||
| chr5:109689844-109689956 | Rare:37 | ||||
| chr5:110738906-110739088 | Common:2; Rare:70 | ||||
| chr5:111092212-111092420 | Common:2; Rare:109; Clinvar:1; Clinvar (benign):4 | ||||
| chr5:111512406-111512826 | Common:4; Rare:142 |