| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:41604824-41605026 | Common:3; Rare:43 | ||||
| chr14:49619013-49619366 | Common:1; Rare:96 | ||||
| chr14:49622008-49622225 | Rare:70; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr14:49633419-49633488 | Rare:25; Clinvar:1 | ||||
| chr14:49633917-49634064 | Common:1; Rare:60; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr14:49862651-49863020 | Common:1; Rare:169 | ||||
| chr14:49868124-49868398 | Common:2; Rare:62 | ||||
| chr14:51593541-51593611 | Common:2; Rare:9 | ||||
| chr14:51596550-51596824 | Common:1; Rare:47 | ||||
| chr14:51650382-51650529 | Common:3; Rare:33 | ||||
| chr14:52080852-52081065 | Common:2; Rare:49 | ||||
| chr14:52781851-52782166 | Common:1; Rare:49 | ||||
| chr14:54487830-54487999 | Common:2; Rare:30 | ||||
| chr14:54651021-54651038 | Rare:4 | ||||
| chr14:55102018-55102248 | Common:1; Rare:38 |