| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:108748686-108748992 | Common:2; Rare:103 | ||||
| chr5:109409858-109410025 | Common:4; Rare:78 | ||||
| chr5:109689827-109689956 | Common:1; Rare:47 | ||||
| chr5:111512438-111512750 | Common:3; Rare:111 | ||||
| chr5:112861160-112861394 | Common:5; Rare:90 | ||||
| chr5:115262837-115262912 | Rare:40 | ||||
| chr5:115841529-115841588 | Common:1; Rare:43 | ||||
| chr5:115841791-115842040 | Common:4; Rare:81 | ||||
| chr5:116085016-116085055 | Rare:21 | ||||
| chr5:116085359-116085481 | Rare:34 | ||||
| chr5:119268573-119268798 | Common:1; Rare:63 | ||||
| chr5:121961669-121962045 | Common:15; Rare:130 | ||||
| chr5:123036663-123037055 | Common:2; Rare:110 | ||||
| chr5:126776951-126777184 | Common:1; Rare:90; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:127030509-127030764 | Common:2; Rare:61 |