| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123700919-123701321 | Common:1; Rare:86; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:123799778-123799853 | Common:1; Rare:11 | ||||
| chr3:124636940-124637244 | Common:2; Rare:59 | ||||
| chr3:124911894-124911913 | Rare:3 | ||||
| chr3:125375234-125375447 | Rare:62 | ||||
| chr3:125520111-125520291 | Rare:70 | ||||
| chr3:125595262-125595403 | Common:2; Rare:42 | ||||
| chr3:126056671-126056832 | Common:1; Rare:34 | ||||
| chr3:126084103-126084223 | Common:1; Rare:53 | ||||
| chr3:127598267-127598469 | Common:2; Rare:59 | ||||
| chr3:127672818-127673026 | Common:3; Rare:99 | ||||
| chr3:127677275-127677524 | Common:1; Rare:73 | ||||
| chr3:127822314-127822668 | Common:1; Rare:87 | ||||
| chr3:128052170-128052504 | Common:2; Rare:111 | ||||
| chr3:128064685-128064902 | Common:1; Rare:43 |