| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:113297020-113297294 | Common:1; Rare:110 | ||||
| chr13:113449113-113449381 | Common:1; Rare:64 | ||||
| chr13:113490679-113491165 | Common:4; Rare:183 | ||||
| chr13:113584497-113584733 | Rare:65 | ||||
| chr13:113864068-113864142 | Rare:19 | ||||
| chr13:114281531-114281721 | Common:1; Rare:106 | ||||
| chr13:114314239-114314580 | Rare:109 | ||||
| chr14:20343408-20343680 | Common:7; Rare:139 | ||||
| chr14:20413117-20413238 | Common:1; Rare:20 | ||||
| chr14:20454714-20455703 | Common:7; Rare:267 | ||||
| chr14:20461734-20462001 | Common:2; Rare:62 | ||||
| chr14:20684388-20684725 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:20989615-20990069 | Common:8; Rare:117 | ||||
| chr14:21211551-21211871 | Common:3; Rare:85 | ||||
| chr14:21262306-21262415 | Rare:21 |