| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110163461-110163761 | Common:6; Rare:56; Clinvar (benign):1 | ||||
| chr13:110305437-110305757 | Common:1; Rare:49 | ||||
| chr13:110307015-110307527 | Common:6; Rare:158; Clinvar:3; Clinvar (benign):9 | ||||
| chr13:110307689-110307931 | Common:3; Rare:79 | ||||
| chr13:110430387-110430598 | Common:2; Rare:56; Clinvar (benign):3 | ||||
| chr13:110561664-110561893 | Common:5; Rare:81 | ||||
| chr13:110615401-110615647 | Common:2; Rare:88 | ||||
| chr13:111202886-111203098 | Common:1; Rare:27 | ||||
| chr13:112979250-112979394 | Common:2; Rare:28 | ||||
| chr13:113208620-113208743 | Rare:76 | ||||
| chr13:113863841-113864205 | Common:3; Rare:91 | ||||
| chr13:114281348-114281654 | Common:5; Rare:126 | ||||
| chr14:20343184-20343669 | Common:12; Rare:291 | ||||
| chr14:20454772-20455290 | Common:7; Rare:137 | ||||
| chr14:20683987-20684238 | Common:16; Rare:136; Clinvar:1; Clinvar (benign):1 |