| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:139556388-139556567 | Rare:23 | ||||
| chr4:140373401-140373696 | Common:2; Rare:122 | ||||
| chr4:145098156-145098322 | Rare:59 | ||||
| chr4:152679959-152680144 | Rare:32 | ||||
| chr4:173370690-173370961 | Common:2; Rare:67 | ||||
| chr4:173530195-173530468 | Common:2; Rare:61 | ||||
| chr4:174283643-174283739 | Rare:19 | ||||
| chr4:184649442-184649756 | Common:4; Rare:101 | ||||
| chr4:185203946-185204083 | Rare:49 | ||||
| chr5:218134-218338 | Common:2; Rare:71; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:443074-443287 | Common:10; Rare:98 | ||||
| chr5:1344854-1344906 | Rare:15 | ||||
| chr5:6633022-6633442 | Common:8; Rare:130; Clinvar:9; Clinvar (benign):3 | ||||
| chr5:7869000-7869204 | Common:2; Rare:103; Clinvar (benign):1 | ||||
| chr5:10353830-10353910 | Common:1; Rare:32 |