| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:40797960-40798572 | Common:15; Rare:909 | ||||
| chr5:40798587-40798914 | Common:4; Rare:164 | ||||
| chr5:40801930-40802414 | Common:8; Rare:317 | ||||
| chr5:40834155-40834969 | Common:15; Rare:480 | ||||
| chr5:40834966-40835858 | Common:31; Rare:1181 | ||||
| chr5:40840880-40841376 | Common:1; Rare:138 | ||||
| chr5:40841382-40841950 | Common:10; Rare:327 | ||||
| chr5:41869810-41870240 | Rare:167 | ||||
| chr5:41870310-41871314 | Common:14; Rare:791; Clinvar:21; Clinvar (benign):14 | ||||
| chr5:41903896-41904438 | Common:9; Rare:673 | ||||
| chr5:41904414-41904814 | Common:1; Rare:116 | ||||
| chr5:41924497-41924963 | Common:6; Rare:132 | ||||
| chr5:41924898-41925018 | Common:1; Rare:20 | ||||
| chr5:41925032-41925446 | Common:9; Rare:529 | ||||
| chr5:41925400-41925847 | Rare:171 |