| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:95157236-95157992 | Common:15; Rare:575; Clinvar:5; Clinvar (benign):5 | ||||
| chr14:95307446-95308005 | Common:5; Rare:306 | ||||
| chr14:95319116-95319721 | Common:5; Rare:164 | ||||
| chr14:95319736-95320210 | Common:11; Rare:206 | ||||
| chr14:95532751-95533705 | Common:8; Rare:454 | ||||
| chr14:95534505-95535119 | Common:17; Rare:605; Clinvar (benign):12 | ||||
| chr14:96204630-96204935 | Common:9; Rare:273 | ||||
| chr14:96363163-96363622 | Common:6; Rare:354 | ||||
| chr14:96363962-96364362 | Common:2; Rare:135 | ||||
| chr14:96391433-96392285 | Common:8; Rare:429 | ||||
| chr14:96501561-96501881 | Rare:80 | ||||
| chr14:96501928-96502657 | Common:5; Rare:494 | ||||
| chr14:96502697-96503101 | Common:12; Rare:234 | ||||
| chr14:96797326-96797501 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:99270821-99271343 | Common:5; Rare:175 |