| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:40798129-40798345 | Rare:85 | ||||
| chr5:41870364-41870440 | Rare:36; Clinvar:1 | ||||
| chr5:41870499-41870572 | Common:1; Rare:16; Clinvar (benign):1 | ||||
| chr5:41904017-41904370 | Common:1; Rare:104 | ||||
| chr5:41925192-41925306 | Common:1; Rare:44 | ||||
| chr5:43043143-43043261 | Rare:22 | ||||
| chr5:43064836-43065137 | Rare:71 | ||||
| chr5:43067351-43067577 | Rare:36 | ||||
| chr5:43121420-43121648 | Common:1; Rare:86 | ||||
| chr5:43313385-43313657 | Common:3; Rare:73 | ||||
| chr5:43483837-43483936 | Common:1; Rare:38 | ||||
| chr5:43515133-43515264 | Common:2; Rare:46 | ||||
| chr5:43602885-43603280 | Rare:97 | ||||
| chr5:44389411-44389631 | Rare:31 | ||||
| chr5:44808718-44809040 | Common:2; Rare:120 |