| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:36876950-36877190 | Rare:112; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:37248800-37249200 | Common:6; Rare:140 | ||||
| chr5:37249266-37249464 | Common:1; Rare:117; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:37371008-37371179 | Rare:113 | ||||
| chr5:37379057-37379372 | Common:3; Rare:76 | ||||
| chr5:38556593-38556844 | Common:4; Rare:181 | ||||
| chr5:38845704-38846146 | Common:4; Rare:206 | ||||
| chr5:39074367-39074559 | Common:2; Rare:161 | ||||
| chr5:40798148-40798438 | Common:2; Rare:203 | ||||
| chr5:40835149-40835423 | Common:4; Rare:222 | ||||
| chr5:41904011-41904393 | Common:4; Rare:232 | ||||
| chr5:41925132-41925316 | Common:2; Rare:121 | ||||
| chr5:42811816-42812186 | Common:3; Rare:104 | ||||
| chr5:42825814-42826155 | Common:1; Rare:80 | ||||
| chr5:43064810-43065145 | Common:2; Rare:130 |