| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:103120080-103120436 | Common:1; Rare:89 | ||||
| chr5:103562723-103562914 | Common:7; Rare:73 | ||||
| chr5:107670612-107670653 | Common:1; Rare:17 | ||||
| chr5:108382063-108382165 | Common:1; Rare:35 | ||||
| chr5:108382406-108382550 | Rare:52 | ||||
| chr5:108748673-108748993 | Common:2; Rare:112 | ||||
| chr5:109409286-109409461 | Common:1; Rare:58 | ||||
| chr5:109409849-109410211 | Common:4; Rare:137 | ||||
| chr5:109689236-109689458 | Common:4; Rare:107 | ||||
| chr5:110738906-110739128 | Common:2; Rare:89 | ||||
| chr5:111092231-111092448 | Common:2; Rare:112; Clinvar:1; Clinvar (benign):4 | ||||
| chr5:111224103-111224524 | Common:2; Rare:163 | ||||
| chr5:111512383-111512875 | Common:4; Rare:154 | ||||
| chr5:111756248-111756361 | Common:2; Rare:17 | ||||
| chr5:111757070-111757254 | Common:4; Rare:47 |