| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:95961808-95962012 | Common:1; Rare:52 | ||||
| chr5:96702559-96702874 | Common:1; Rare:79 | ||||
| chr5:97183216-97183515 | Common:4; Rare:106 | ||||
| chr5:100535209-100535399 | Rare:49 | ||||
| chr5:100903192-100903389 | Common:1; Rare:36 | ||||
| chr5:103120116-103120386 | Common:1; Rare:65 | ||||
| chr5:108748686-108748982 | Common:2; Rare:98 | ||||
| chr5:109689804-109689960 | Common:1; Rare:55 | ||||
| chr5:110738923-110739072 | Common:2; Rare:56 | ||||
| chr5:111092238-111092371 | Common:1; Rare:70; Clinvar (benign):2 | ||||
| chr5:111512472-111512780 | Common:3; Rare:119 | ||||
| chr5:112737797-112737888 | Rare:20; Clinvar (benign):1 | ||||
| chr5:112976552-112976832 | Common:2; Rare:123 | ||||
| chr5:115841549-115841625 | Common:1; Rare:42 | ||||
| chr5:115841831-115842016 | Common:3; Rare:61 |