| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:110738888-110739055 | Common:1; Rare:54 | ||||
| chr5:110739411-110739547 | Common:1; Rare:47 | ||||
| chr5:111092159-111092420 | Common:2; Rare:132; Clinvar:3; Clinvar (benign):4 | ||||
| chr5:111224080-111224520 | Common:2; Rare:165 | ||||
| chr5:111512435-111512878 | Common:4; Rare:144 | ||||
| chr5:111512975-111513295 | Common:1; Rare:68 | ||||
| chr5:111756250-111756941 | Common:3; Rare:197 | ||||
| chr5:111757057-111757586 | Common:6; Rare:139 | ||||
| chr5:111757738-111757901 | Common:1; Rare:61 | ||||
| chr5:111758026-111758297 | Common:5; Rare:85 | ||||
| chr5:112419488-112419756 | Common:1; Rare:123 | ||||
| chr5:112707308-112707672 | Common:8; Rare:147; Clinvar:75; Clinvar (benign):15; Clinvar (pathogenic):1 | ||||
| chr5:112737569-112737926 | Rare:85; Clinvar:2; Clinvar (benign):5 | ||||
| chr5:112738314-112738418 | Rare:20 | ||||
| chr5:112861102-112861383 | Common:4; Rare:111 |