| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:73644544-73644659 | Rare:20 | ||||
| chr14:73644809-73645028 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:73713760-73714083 | Common:1; Rare:91 | ||||
| chr14:73714256-73714523 | Common:2; Rare:90 | ||||
| chr14:73759757-73760645 | Common:4; Rare:159 | ||||
| chr14:73787101-73787379 | Common:3; Rare:93 | ||||
| chr14:73787395-73787512 | Common:2; Rare:31 | ||||
| chr14:73851652-73851881 | Common:1; Rare:60 | ||||
| chr14:73851905-73852094 | Common:7; Rare:55 | ||||
| chr14:73852211-73852336 | Common:1; Rare:33 | ||||
| chr14:73886327-73886446 | Rare:21 | ||||
| chr14:73886498-73886990 | Common:5; Rare:145 | ||||
| chr14:73887297-73887375 | Common:1; Rare:21 | ||||
| chr14:73950017-73950461 | Common:6; Rare:182; Clinvar:1; Clinvar (benign):5 | ||||
| chr14:73950512-73950522 | Rare:1 |