| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:114281480-114281682 | Common:2; Rare:111 | ||||
| chr13:114281831-114282065 | Common:5; Rare:111 | ||||
| chr14:20343178-20343644 | Common:12; Rare:273 | ||||
| chr14:20413409-20413569 | Common:3; Rare:48 | ||||
| chr14:20454757-20455281 | Common:7; Rare:136 | ||||
| chr14:20684418-20684735 | Common:2; Rare:61; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:20989739-20990005 | Common:5; Rare:56 | ||||
| chr14:21022251-21022442 | Rare:45 | ||||
| chr14:21024936-21025385 | Common:1; Rare:137 | ||||
| chr14:21025494-21025585 | Common:1; Rare:20 | ||||
| chr14:21025661-21026061 | Common:2; Rare:71 | ||||
| chr14:21070155-21070381 | Common:1; Rare:61 | ||||
| chr14:21456035-21456134 | Common:2; Rare:26 | ||||
| chr14:21476598-21476759 | Rare:70 | ||||
| chr14:21476868-21477271 | Common:2; Rare:131 |