| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:114281867-114282061 | Common:5; Rare:86 | ||||
| chr14:20343161-20343644 | Common:13; Rare:282 | ||||
| chr14:20454747-20455270 | Common:7; Rare:136 | ||||
| chr14:20683976-20684233 | Common:16; Rare:139; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:20684461-20684752 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:20989665-20990002 | Common:7; Rare:71 | ||||
| chr14:21025023-21025290 | Rare:87 | ||||
| chr14:21025494-21025613 | Common:1; Rare:29 | ||||
| chr14:21025677-21026058 | Common:2; Rare:66 | ||||
| chr14:21383938-21384286 | Common:8; Rare:114 | ||||
| chr14:21456042-21456348 | Common:4; Rare:78 | ||||
| chr14:21476598-21476775 | Rare:81 | ||||
| chr14:21476868-21477267 | Common:2; Rare:128 | ||||
| chr14:21511232-21511549 | Rare:97 | ||||
| chr14:21526242-21526459 | Rare:48 |