| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:96204726-96204935 | Common:4; Rare:82 | ||||
| chr14:96363131-96363552 | Common:3; Rare:130 | ||||
| chr14:96502251-96502595 | Common:2; Rare:147 | ||||
| chr14:99480728-99480973 | Common:2; Rare:98 | ||||
| chr14:100065272-100065446 | Rare:26 | ||||
| chr14:100238550-100238867 | Common:3; Rare:93 | ||||
| chr14:100306439-100306699 | Common:3; Rare:92 | ||||
| chr14:100375284-100375755 | Common:4; Rare:80 | ||||
| chr14:100376258-100376521 | Common:3; Rare:85 | ||||
| chr14:101561226-101561499 | Common:1; Rare:82 | ||||
| chr14:101809684-101810056 | Rare:87 | ||||
| chr14:101810287-101810453 | Common:2; Rare:34 | ||||
| chr14:101823776-101823863 | Rare:17 | ||||
| chr14:101964296-101964674 | Common:4; Rare:115; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:102083544-102083983 | Common:3; Rare:179 |