| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:185775242-185775474 | Common:1; Rare:34 | ||||
| chr4:186726620-186726932 | Common:4; Rare:103 | ||||
| chr4:189940588-189940967 | Common:11; Rare:125 | ||||
| chr5:218124-218358 | Common:3; Rare:94; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr5:443080-443280 | Common:10; Rare:93 | ||||
| chr5:892653-892923 | Common:5; Rare:95 | ||||
| chr5:1799791-1799938 | Common:4; Rare:76 | ||||
| chr5:1801335-1801447 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:7869004-7869194 | Common:2; Rare:92; Clinvar (benign):1 | ||||
| chr5:9545977-9546361 | Common:10; Rare:96 | ||||
| chr5:10353597-10353901 | Common:3; Rare:111 | ||||
| chr5:16465734-16465882 | Rare:24 | ||||
| chr5:31532021-31532341 | Common:3; Rare:86 | ||||
| chr5:32174277-32174402 | Common:1; Rare:45 | ||||
| chr5:32444662-32444967 | Common:1; Rare:111 |