| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140107615-140107846 | Rare:83 | ||||
| chr5:140175011-140175268 | Common:1; Rare:64 | ||||
| chr5:140346590-140346721 | Common:1; Rare:36 | ||||
| chr5:140557427-140557555 | Common:2; Rare:76 | ||||
| chr5:140564278-140564559 | Common:2; Rare:70 | ||||
| chr5:140564573-140564837 | Rare:73 | ||||
| chr5:140592091-140592236 | Rare:28 | ||||
| chr5:140647583-140647924 | Common:5; Rare:139; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664753-140664915 | Common:2; Rare:44 | ||||
| chr5:140691305-140691641 | Common:1; Rare:119; Clinvar:9; Clinvar (benign):1 | ||||
| chr5:141320088-141320377 | Common:4; Rare:62 | ||||
| chr5:141320742-141320920 | Common:1; Rare:62 | ||||
| chr5:141636809-141637001 | Common:2; Rare:83 | ||||
| chr5:141682195-141682327 | Common:1; Rare:42 | ||||
| chr5:141923750-141923916 | Common:1; Rare:49 |