| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:93332872-93333484 | Common:16; Rare:1005 | ||||
| chr14:94026062-94026462 | Common:5; Rare:179 | ||||
| chr14:94080368-94080808 | Common:14; Rare:209 | ||||
| chr14:94081063-94081463 | Common:29; Rare:549 | ||||
| chr14:94081467-94081867 | Common:2; Rare:70 | ||||
| chr14:94110530-94110840 | Common:3; Rare:111 | ||||
| chr14:94129510-94129810 | Common:9; Rare:206 | ||||
| chr14:94173830-94174450 | Common:8; Rare:325 | ||||
| chr14:95156800-95158230 | Common:40; Rare:1397; Clinvar:4; Clinvar (benign):3 | ||||
| chr14:95319679-95320160 | Common:17; Rare:315 | ||||
| chr14:95533250-95534370 | Common:10; Rare:558 | ||||
| chr14:95534473-95535191 | Common:29; Rare:1169; Clinvar (benign):24 | ||||
| chr14:96363266-96363669 | Common:8; Rare:696 | ||||
| chr14:96363968-96364428 | Common:3; Rare:229 | ||||
| chr14:96391292-96391692 | Common:1; Rare:89 |