| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77799991-77800151 | Rare:31 | ||||
| chr14:78170291-78170412 | Rare:24 | ||||
| chr14:80210976-80211126 | Rare:20 | ||||
| chr14:80941690-80941940 | Common:3; Rare:55 | ||||
| chr14:81220088-81220441 | Common:2; Rare:105 | ||||
| chr14:81220707-81221175 | Common:3; Rare:183 | ||||
| chr14:81221279-81221450 | Common:1; Rare:41 | ||||
| chr14:81436433-81436636 | Common:1; Rare:76 | ||||
| chr14:81533783-81534163 | Rare:100 | ||||
| chr14:85530033-85530205 | Common:1; Rare:38 | ||||
| chr14:87992750-87993096 | Common:3; Rare:133; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr14:88551414-88551609 | Common:2; Rare:50 | ||||
| chr14:88554668-88554784 | Common:3; Rare:31 | ||||
| chr14:88562898-88563279 | Rare:153 | ||||
| chr14:88563445-88563578 | Rare:60 |