| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:111092221-111092456 | Common:2; Rare:120; Clinvar:1; Clinvar (benign):4 | ||||
| chr5:111224106-111224561 | Common:2; Rare:173 | ||||
| chr5:111512385-111512874 | Common:4; Rare:153 | ||||
| chr5:111756166-111756344 | Common:2; Rare:27 | ||||
| chr5:111757031-111757885 | Common:7; Rare:270 | ||||
| chr5:111757936-111758144 | Common:2; Rare:70 | ||||
| chr5:111758148-111758242 | Common:1; Rare:27 | ||||
| chr5:112419245-112419303 | Common:1; Rare:24 | ||||
| chr5:112707379-112707821 | Common:7; Rare:186; Clinvar:92; Clinvar (benign):17; Clinvar (pathogenic):1 | ||||
| chr5:112737687-112738213 | Rare:122; Clinvar:4; Clinvar (benign):5 | ||||
| chr5:112861049-112861386 | Common:5; Rare:122 | ||||
| chr5:112976494-112976923 | Common:3; Rare:210 | ||||
| chr5:113513624-113513755 | Rare:47 | ||||
| chr5:115169646-115169789 | Rare:43 | ||||
| chr5:115169810-115170239 | Rare:152 |