| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:119431906-119432131 | Rare:64 | ||||
| chr2:119679061-119679288 | Common:4; Rare:66 | ||||
| chr2:119759431-119759677 | Common:1; Rare:73 | ||||
| chr2:119759683-119760025 | Common:2; Rare:97 | ||||
| chr2:120012797-120013164 | Common:3; Rare:147 | ||||
| chr2:120013333-120013516 | Common:1; Rare:56 | ||||
| chr2:120223096-120223235 | Common:4; Rare:47 | ||||
| chr2:120223323-120223585 | Common:1; Rare:94 | ||||
| chr2:120252544-120252968 | Common:3; Rare:134 | ||||
| chr2:120253768-120253982 | Rare:30 | ||||
| chr2:121530355-121530431 | Rare:24 | ||||
| chr2:121530514-121530966 | Common:8; Rare:252; Clinvar (pathogenic):12 | ||||
| chr2:121531116-121531310 | Common:4; Rare:116 | ||||
| chr2:121648821-121649162 | Common:3; Rare:79 | ||||
| chr2:121649394-121649711 | Common:2; Rare:95 |