| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23034579-23034810 | Rare:61 | ||||
| chr14:23066044-23066183 | Common:1; Rare:38 | ||||
| chr14:23066233-23066656 | Common:2; Rare:80 | ||||
| chr14:23070373-23070827 | Common:2; Rare:97 | ||||
| chr14:23071235-23071324 | Rare:23 | ||||
| chr14:23071477-23071808 | Common:1; Rare:98 | ||||
| chr14:23094216-23094276 | Rare:5 | ||||
| chr14:23094510-23094701 | Common:2; Rare:53 | ||||
| chr14:23094948-23095615 | Common:3; Rare:264 | ||||
| chr14:23286106-23286304 | Rare:45 | ||||
| chr14:23306565-23306935 | Common:1; Rare:76 | ||||
| chr14:23321107-23321558 | Common:2; Rare:136; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr14:23321560-23322298 | Common:4; Rare:223; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:23352798-23352941 | Rare:39 | ||||
| chr14:23365021-23365258 | Rare:48 |