| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:136194447-136194489 | Common:1; Rare:16 | ||||
| chr3:136194928-136195111 | Rare:64; Clinvar:1 | ||||
| chr3:136195424-136195499 | Rare:20 | ||||
| chr3:136195728-136196055 | Common:2; Rare:142 | ||||
| chr3:136196191-136197131 | Common:2; Rare:317 | ||||
| chr3:136197218-136197334 | Rare:27 | ||||
| chr3:136250225-136250406 | Common:3; Rare:79; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr3:136250453-136250768 | Common:3; Rare:112; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:136250961-136251189 | Common:1; Rare:52 | ||||
| chr3:136752295-136752898 | Common:1; Rare:215 | ||||
| chr3:136818300-136818529 | Rare:39 | ||||
| chr3:136818960-136819228 | Common:4; Rare:119 | ||||
| chr3:136861873-136862407 | Common:2; Rare:165 | ||||
| chr3:136862644-136862891 | Common:3; Rare:71 | ||||
| chr3:138174622-138174975 | Common:4; Rare:119 |