| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:121545956-121546111 | Common:1; Rare:42 | ||||
| chr3:121749199-121749300 | Rare:23 | ||||
| chr3:121749463-121749530 | Rare:13 | ||||
| chr3:121749623-121750021 | Common:1; Rare:91 | ||||
| chr3:121834964-121835248 | Common:3; Rare:96; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122325081-122325372 | Common:1; Rare:78; Clinvar (pathogenic):1 | ||||
| chr3:122366429-122366798 | Common:1; Rare:56 | ||||
| chr3:122383183-122383351 | Common:2; Rare:50 | ||||
| chr3:122383360-122383431 | Rare:9 | ||||
| chr3:122384098-122384268 | Rare:67 | ||||
| chr3:122416039-122416229 | Common:1; Rare:61 | ||||
| chr3:122514800-122514994 | Common:2; Rare:60 | ||||
| chr3:122564230-122564466 | Common:3; Rare:71 | ||||
| chr3:122680664-122680886 | Rare:69 | ||||
| chr3:122681170-122681257 | Rare:19 |