| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46296669-46296765 | Common:2; Rare:39 | ||||
| chr22:46762496-46762741 | Common:3; Rare:91 | ||||
| chr22:46763182-46763292 | Common:1; Rare:34 | ||||
| chr22:49918412-49918702 | Common:1; Rare:109 | ||||
| chr22:50190387-50190713 | Common:4; Rare:98 | ||||
| chr22:50192473-50192614 | Common:1; Rare:25 | ||||
| chr22:50244969-50245108 | Common:1; Rare:56 | ||||
| chr22:50525593-50525758 | Common:3; Rare:86; Clinvar:2 | ||||
| chr22:50530958-50531246 | Common:1; Rare:96 | ||||
| chr22:50582784-50583145 | Common:7; Rare:122; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628076-50628276 | Common:9; Rare:96; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783596-50783821 | Common:2; Rare:75 | ||||
| chr3:3110232-3110487 | Rare:47 | ||||
| chr3:3126775-3127067 | Common:4; Rare:122; Clinvar (benign):4 | ||||
| chr3:9362811-9363098 | Common:2; Rare:87 |