| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36242123-36242325 | Common:1; Rare:55 | ||||
| chr5:36876657-36876889 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371024-37371360 | Common:2; Rare:87 | ||||
| chr5:37379187-37379364 | Rare:46 | ||||
| chr5:38845779-38846053 | Common:1; Rare:71 | ||||
| chr5:39074329-39074539 | Common:1; Rare:104 | ||||
| chr5:39424935-39425285 | Common:3; Rare:73 | ||||
| chr5:40798152-40798376 | Common:1; Rare:85 | ||||
| chr5:40835151-40835406 | Common:2; Rare:107 | ||||
| chr5:41870364-41870553 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:41904011-41904389 | Common:2; Rare:121 | ||||
| chr5:43067428-43067565 | Rare:25 | ||||
| chr5:43121420-43121648 | Common:1; Rare:86 | ||||
| chr5:43313364-43313634 | Common:3; Rare:73 | ||||
| chr5:43483831-43483970 | Common:1; Rare:48 |