| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:74291906-74292267 | Common:4; Rare:108 | ||||
| chr18:74496021-74496421 | Common:4; Rare:130 | ||||
| chr18:74597579-74597929 | Common:2; Rare:97 | ||||
| chr18:76495164-76495506 | Common:2; Rare:92 | ||||
| chr18:76822226-76822645 | Common:11; Rare:119 | ||||
| chr18:79069015-79069282 | Common:8; Rare:115 | ||||
| chr18:79679150-79679566 | Common:3; Rare:182 | ||||
| chr18:79988271-79988715 | Common:5; Rare:150; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:344784-344951 | Common:3; Rare:61 | ||||
| chr19:409059-409327 | Common:2; Rare:84 | ||||
| chr19:507267-507512 | Common:2; Rare:83 | ||||
| chr19:572326-572629 | Rare:158 | ||||
| chr19:633494-633745 | Common:8; Rare:117 | ||||
| chr19:663132-663461 | Common:2; Rare:130 | ||||
| chr19:680458-680753 | Common:2; Rare:101 |