| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36876652-36876812 | Rare:45 | ||||
| chr5:37248920-37249100 | Common:2; Rare:37 | ||||
| chr5:37249314-37249611 | Common:1; Rare:106; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371068-37371240 | Rare:52 | ||||
| chr5:38556602-38556967 | Common:2; Rare:127 | ||||
| chr5:39074346-39074658 | Common:2; Rare:125 | ||||
| chr5:39424360-39424620 | Common:2; Rare:29 | ||||
| chr5:39425042-39425386 | Common:2; Rare:75 | ||||
| chr5:40679695-40679924 | Common:1; Rare:46 | ||||
| chr5:40755889-40756093 | Rare:54 | ||||
| chr5:40798094-40798457 | Common:2; Rare:136 | ||||
| chr5:40834425-40835066 | Common:9; Rare:283 | ||||
| chr5:40835167-40835473 | Common:4; Rare:117 | ||||
| chr5:41870360-41870562 | Common:1; Rare:68; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:41903913-41904395 | Common:2; Rare:148 |