| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:20684473-20684601 | Common:1; Rare:20; Clinvar (benign):1 | ||||
| chr14:20802330-20802606 | Common:2; Rare:48 | ||||
| chr14:20989665-20990076 | Common:7; Rare:105 | ||||
| chr14:21025006-21025191 | Rare:68 | ||||
| chr14:21025422-21025814 | Common:2; Rare:91 | ||||
| chr14:21070155-21070381 | Common:1; Rare:61 | ||||
| chr14:21383931-21384083 | Common:1; Rare:59 | ||||
| chr14:21456042-21456229 | Common:3; Rare:52 | ||||
| chr14:21476619-21476714 | Rare:46 | ||||
| chr14:21476868-21477267 | Common:2; Rare:128 | ||||
| chr14:21511284-21511357 | Rare:20 | ||||
| chr14:21526207-21526412 | Rare:42 | ||||
| chr14:22589116-22589463 | Common:4; Rare:113 | ||||
| chr14:22766554-22766701 | Common:1; Rare:77 | ||||
| chr14:22871651-22871861 | Rare:52 |