| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:40755760-40756040 | Rare:62 | ||||
| chr5:40798130-40798401 | Common:1; Rare:103 | ||||
| chr5:40835181-40835385 | Common:2; Rare:81 | ||||
| chr5:40841235-40841450 | Rare:62 | ||||
| chr5:41870360-41870591 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:41904008-41904401 | Common:2; Rare:129 | ||||
| chr5:43043207-43043316 | Common:1; Rare:22 | ||||
| chr5:43064815-43065144 | Common:1; Rare:78 | ||||
| chr5:43067348-43067516 | Rare:23 | ||||
| chr5:43121419-43121655 | Common:1; Rare:88 | ||||
| chr5:43191956-43192257 | Common:2; Rare:72 | ||||
| chr5:43313386-43313652 | Common:3; Rare:70 | ||||
| chr5:43483822-43483955 | Common:3; Rare:46 | ||||
| chr5:43515133-43515307 | Common:3; Rare:63 | ||||
| chr5:43602628-43602741 | Rare:18 |