| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:112969072-112969356 | Common:2; Rare:77 | ||||
| chr13:113158525-113158663 | Common:2; Rare:44 | ||||
| chr13:113158960-113159118 | Common:1; Rare:39 | ||||
| chr13:113208625-113208752 | Rare:73 | ||||
| chr13:113209475-113209624 | Common:3; Rare:47 | ||||
| chr13:113490683-113491034 | Common:1; Rare:128 | ||||
| chr13:114281299-114281654 | Common:5; Rare:140 | ||||
| chr14:20343193-20343652 | Common:12; Rare:269 | ||||
| chr14:20454768-20455289 | Common:7; Rare:138 | ||||
| chr14:20684148-20684756 | Common:7; Rare:127; Clinvar:3; Clinvar (benign):9 | ||||
| chr14:20688583-20688882 | Common:2; Rare:57 | ||||
| chr14:20891345-20891407 | Rare:17 | ||||
| chr14:21024050-21024327 | Common:3; Rare:48 | ||||
| chr14:21024965-21025228 | Rare:96 | ||||
| chr14:21025677-21025767 | Rare:20 |