| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:89618967-89619335 | Common:1; Rare:119 | ||||
| chr14:89619479-89619521 | Rare:6 | ||||
| chr14:89954429-89954970 | Common:3; Rare:173 | ||||
| chr14:89955791-89956010 | Common:9; Rare:76; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:89956192-89956271 | Rare:36 | ||||
| chr14:89956325-89956587 | Common:4; Rare:67; Clinvar (benign):3 | ||||
| chr14:90256439-90256635 | Common:2; Rare:65 | ||||
| chr14:90288740-90288891 | Rare:51 | ||||
| chr14:90331595-90331747 | Rare:38 | ||||
| chr14:90331876-90332411 | Common:1; Rare:139 | ||||
| chr14:90396703-90397210 | Common:7; Rare:225; Clinvar (benign):2 | ||||
| chr14:90397773-90397978 | Common:1; Rare:56 | ||||
| chr14:90398059-90398179 | Common:3; Rare:26 | ||||
| chr14:90398684-90398720 | Rare:5 | ||||
| chr14:91060113-91060365 | Common:2; Rare:84 |