| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20343186-20343679 | Common:12; Rare:295 | ||||
| chr14:20413420-20413562 | Common:3; Rare:44 | ||||
| chr14:20454734-20455629 | Common:7; Rare:234 | ||||
| chr14:20461400-20461728 | Common:2; Rare:90 | ||||
| chr14:20461817-20462020 | Common:2; Rare:47 | ||||
| chr14:20683963-20684244 | Common:17; Rare:145; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:20684461-20684701 | Common:1; Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:20989663-20989804 | Common:4; Rare:28 | ||||
| chr14:20989960-20990076 | Common:2; Rare:50 | ||||
| chr14:21070141-21070381 | Common:1; Rare:67 | ||||
| chr14:21103612-21104209 | Common:5; Rare:140 | ||||
| chr14:21104708-21104784 | Rare:14 | ||||
| chr14:21269514-21269873 | Common:2; Rare:119 | ||||
| chr14:21383864-21384057 | Common:1; Rare:67 | ||||
| chr14:21384207-21384424 | Rare:75 |