| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:113759137-113759267 | Rare:41 | ||||
| chr13:113863831-113864160 | Common:3; Rare:78 | ||||
| chr13:114281519-114281648 | Common:2; Rare:70 | ||||
| chr14:20343162-20343655 | Common:13; Rare:286 | ||||
| chr14:20413413-20413590 | Common:3; Rare:52 | ||||
| chr14:20455042-20455368 | Common:2; Rare:89 | ||||
| chr14:20455454-20455564 | Rare:28 | ||||
| chr14:20456437-20456704 | Common:1; Rare:73; Clinvar:1 | ||||
| chr14:20684428-20684686 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:20999073-20999321 | Rare:49 | ||||
| chr14:21024981-21025187 | Rare:77 | ||||
| chr14:21383938-21384083 | Common:1; Rare:55 | ||||
| chr14:21476868-21477253 | Common:1; Rare:119 | ||||
| chr14:22589048-22589254 | Common:2; Rare:69 | ||||
| chr14:22766554-22766704 | Common:1; Rare:78 |