| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:96363962-96364261 | Common:1; Rare:65 | ||||
| chr14:96391587-96391691 | Common:1; Rare:20 | ||||
| chr14:96391715-96392166 | Common:2; Rare:128 | ||||
| chr14:96501675-96501819 | Rare:39 | ||||
| chr14:96501826-96501973 | Rare:41 | ||||
| chr14:96501978-96502136 | Rare:50 | ||||
| chr14:96502152-96502570 | Common:2; Rare:160 | ||||
| chr14:96502743-96503163 | Common:4; Rare:120 | ||||
| chr14:96797194-96797484 | Common:2; Rare:84; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:99480145-99480435 | Common:4; Rare:97 | ||||
| chr14:99480727-99481026 | Common:2; Rare:113 | ||||
| chr14:99481069-99481536 | Common:1; Rare:126 | ||||
| chr14:99481624-99481747 | Rare:30 | ||||
| chr14:99481903-99482003 | Rare:17 | ||||
| chr14:99523040-99523259 | Common:3; Rare:32 |