| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:88551935-88552335 | Rare:78 | ||||
| chr14:88554774-88555250 | Common:6; Rare:191 | ||||
| chr14:88562765-88563165 | Rare:655 | ||||
| chr14:88563328-88563728 | Common:1; Rare:284; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:88792770-88793175 | Rare:470 | ||||
| chr14:88824291-88824799 | Common:12; Rare:624; Clinvar:14; Clinvar (benign):5 | ||||
| chr14:89417059-89418108 | Common:11; Rare:339 | ||||
| chr14:89954520-89955166 | Common:15; Rare:824 | ||||
| chr14:89955235-89955635 | Rare:68 | ||||
| chr14:89955700-89956186 | Common:41; Rare:423; Clinvar:12; Clinvar (benign):4 | ||||
| chr14:89956219-89956619 | Common:5; Rare:131; Clinvar (benign):3 | ||||
| chr14:89956532-89956673 | Common:4; Rare:29; Clinvar (benign):4 | ||||
| chr14:90256315-90256715 | Common:8; Rare:220 | ||||
| chr14:90331550-90331850 | Common:1; Rare:160 | ||||
| chr14:90331871-90332271 | Common:7; Rare:632 |