| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:111153529-111153721 | Common:2; Rare:96 | ||||
| chr13:113122652-113122847 | Common:1; Rare:50; Clinvar (benign):1 | ||||
| chr13:113208620-113208775 | Rare:91 | ||||
| chr13:113364070-113364463 | Common:2; Rare:29 | ||||
| chr13:113490699-113491021 | Common:1; Rare:117 | ||||
| chr13:113759053-113759288 | Common:1; Rare:61 | ||||
| chr13:113863844-113864160 | Common:3; Rare:77 | ||||
| chr13:114281501-114281684 | Common:2; Rare:105 | ||||
| chr14:20333260-20333461 | Common:1; Rare:40 | ||||
| chr14:20343161-20343655 | Common:13; Rare:286 | ||||
| chr14:20413161-20413233 | Common:1; Rare:11 | ||||
| chr14:20413413-20413551 | Common:3; Rare:42 | ||||
| chr14:20454772-20455270 | Common:7; Rare:131 | ||||
| chr14:20684301-20684386 | Common:1; Rare:20; Clinvar (benign):2 | ||||
| chr14:20684426-20684756 | Common:3; Rare:65; Clinvar:1; Clinvar (benign):3 |