| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:95822671-95822993 | Rare:70 | ||||
| chr5:95961802-95962012 | Common:1; Rare:52 | ||||
| chr5:96702545-96702874 | Common:1; Rare:80 | ||||
| chr5:96935840-96936136 | Common:8; Rare:100 | ||||
| chr5:97183209-97183536 | Common:4; Rare:117 | ||||
| chr5:98928921-98929188 | Common:3; Rare:117 | ||||
| chr5:100535197-100535398 | Rare:52 | ||||
| chr5:100903231-100903389 | Rare:31 | ||||
| chr5:102755042-102755331 | Common:2; Rare:97 | ||||
| chr5:103120116-103120372 | Common:1; Rare:60 | ||||
| chr5:103258477-103258777 | Common:1; Rare:93 | ||||
| chr5:108748679-108748991 | Common:2; Rare:107 | ||||
| chr5:110738915-110739061 | Common:1; Rare:49 | ||||
| chr5:112737771-112737911 | Rare:32; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:115544740-115545007 | Common:2; Rare:105 |