| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:54396734-54397077 | Common:2; Rare:96 | ||||
| chr14:54441248-54441753 | Common:1; Rare:154 | ||||
| chr14:54488737-54488915 | Common:2; Rare:48 | ||||
| chr14:54488928-54489091 | Common:1; Rare:57 | ||||
| chr14:54509620-54509956 | Common:6; Rare:119 | ||||
| chr14:54567016-54567186 | Rare:46 | ||||
| chr14:54568108-54568317 | Common:2; Rare:51 | ||||
| chr14:54902824-54902962 | Rare:37; Clinvar (benign):1 | ||||
| chr14:55027043-55027617 | Common:4; Rare:125 | ||||
| chr14:55051425-55051761 | Common:1; Rare:147 | ||||
| chr14:55129088-55129299 | Common:1; Rare:58 | ||||
| chr14:55191513-55191768 | Common:5; Rare:62 | ||||
| chr14:55271153-55271471 | Common:2; Rare:103 | ||||
| chr14:55411800-55411905 | Common:1; Rare:43 | ||||
| chr14:55411907-55411949 | Rare:24 |