| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:19251525-19251818 | Common:6; Rare:92 | ||||
| chr1:160343245-160343372 | Rare:43 | ||||
| chr10:12195887-12196219 | Rare:78 | ||||
| chr11:809810-810028 | Common:2; Rare:102 | ||||
| chr11:6481310-6481527 | Common:4; Rare:89 | ||||
| chr11:66480247-66480444 | Common:1; Rare:51 | ||||
| chr11:68903812-68903916 | Common:1; Rare:42; Clinvar (benign):2 | ||||
| chr14:75660871-75660991 | Rare:24 | ||||
| chr16:67481136-67481377 | Common:1; Rare:77 | ||||
| chr18:36828995-36829153 | Common:3; Rare:64 | ||||
| chr19:39391125-39391412 | Common:1; Rare:116 | ||||
| chr22:30607027-30607262 | Common:3; Rare:71; Clinvar:3; Clinvar (benign):3 | ||||
| chr4:109560030-109560297 | Common:5; Rare:87 | ||||
| chr4:144645885-144646190 | Common:1; Rare:81 | ||||
| chr5:218151-218343 | Common:2; Rare:69; Clinvar:1; Clinvar (benign):2 |