| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:22794460-22794830 | Rare:67 | ||||
| chr14:22795983-22796354 | Common:9; Rare:106 | ||||
| chr14:22796464-22796897 | Common:2; Rare:131 | ||||
| chr14:22797387-22797787 | Common:6; Rare:91 | ||||
| chr14:22803130-22804014 | Common:18; Rare:263 | ||||
| chr14:22811061-22811461 | Common:5; Rare:183 | ||||
| chr14:22811642-22812042 | Common:12; Rare:95 | ||||
| chr14:22813230-22813600 | Common:5; Rare:94; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr14:22824569-22825288 | Common:16; Rare:215 | ||||
| chr14:22838464-22838864 | Common:2; Rare:110 | ||||
| chr14:22853168-22853650 | Common:7; Rare:152 | ||||
| chr14:22886813-22887173 | Common:1; Rare:80 | ||||
| chr14:22887408-22887583 | Rare:47 | ||||
| chr14:22888016-22888416 | Common:3; Rare:107 | ||||
| chr14:22955833-22956233 | Rare:107 |