| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40570560-40570850 | Common:2; Rare:93; Clinvar (pathogenic):1 | ||||
| chr19:40576620-40577000 | Common:6; Rare:106 | ||||
| chr19:40596970-40597234 | Rare:82 | ||||
| chr19:40598124-40598526 | Rare:89 | ||||
| chr19:40689451-40689851 | Common:5; Rare:119 | ||||
| chr19:40690640-40690864 | Common:3; Rare:52 | ||||
| chr19:40715069-40715269 | Rare:55 | ||||
| chr19:40715769-40715939 | Common:3; Rare:36 | ||||
| chr19:40716872-40717155 | Common:1; Rare:89 | ||||
| chr19:40717279-40717390 | Common:1; Rare:54 | ||||
| chr19:40750397-40750606 | Common:4; Rare:66 | ||||
| chr19:40750647-40750952 | Common:2; Rare:65 | ||||
| chr19:40751064-40751339 | Common:3; Rare:79 | ||||
| chr19:40751623-40751838 | Rare:46 | ||||
| chr19:40777865-40778376 | Common:1; Rare:136 |