| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:54102651-54102891 | Common:6; Rare:117 | ||||
| chr19:54115250-54115540 | Common:3; Rare:102; Clinvar (benign):3 | ||||
| chr19:54115628-54115800 | Common:2; Rare:84; Clinvar:8 | ||||
| chr19:54136991-54137270 | Common:10; Rare:134 | ||||
| chr19:54159700-54160153 | Common:1; Rare:291 | ||||
| chr19:54189106-54189458 | Common:2; Rare:123 | ||||
| chr19:54189520-54190355 | Common:15; Rare:431 | ||||
| chr19:54191137-54191343 | Common:6; Rare:128 | ||||
| chr19:54200619-54200927 | Common:10; Rare:208 | ||||
| chr19:54448984-54449301 | Common:8; Rare:173 | ||||
| chr19:54449376-54449666 | Common:8; Rare:129 | ||||
| chr19:55079951-55080563 | Common:3; Rare:168 | ||||
| chr19:55117550-55117990 | Common:15; Rare:228 | ||||
| chr19:55146876-55147031 | Common:3; Rare:96; Clinvar:2; Clinvar (benign):5 | ||||
| chr19:55160630-55160970 | Common:3; Rare:133; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):1 |