| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:112707748-112707809 | Rare:22; Clinvar:9; Clinvar (benign):1 | ||||
| chr5:112737722-112738014 | Rare:78; Clinvar:4; Clinvar (benign):4 | ||||
| chr5:112976445-112976851 | Common:3; Rare:180 | ||||
| chr5:113294595-113294681 | Rare:30 | ||||
| chr5:114433277-114433511 | Rare:54 | ||||
| chr5:115262837-115262888 | Rare:25 | ||||
| chr5:115816510-115816645 | Common:1; Rare:35 | ||||
| chr5:115816649-115816752 | Rare:20 | ||||
| chr5:115841484-115842094 | Common:8; Rare:260 | ||||
| chr5:116085425-116085462 | Rare:5 | ||||
| chr5:116573903-116573990 | Common:1; Rare:26 | ||||
| chr5:119070840-119071191 | Common:4; Rare:107 | ||||
| chr5:119071362-119071422 | Rare:28 | ||||
| chr5:119268586-119268821 | Common:1; Rare:66 | ||||
| chr5:119355819-119356019 | Common:2; Rare:51 |