| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:121749659-121750126 | Common:3; Rare:116 | ||||
| chr3:121834906-121835326 | Common:4; Rare:133; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122022167-122022353 | Common:4; Rare:52 | ||||
| chr3:122055306-122055385 | Rare:16 | ||||
| chr3:122077222-122077546 | Common:2; Rare:44 | ||||
| chr3:122077759-122078082 | Common:1; Rare:60 | ||||
| chr3:122078374-122078419 | Rare:12 | ||||
| chr3:122383141-122383419 | Common:2; Rare:75 | ||||
| chr3:122383995-122384372 | Common:4; Rare:129 | ||||
| chr3:122415906-122416278 | Common:1; Rare:114 | ||||
| chr3:122416340-122416511 | Common:4; Rare:31 | ||||
| chr3:122514547-122514699 | Common:2; Rare:43 | ||||
| chr3:122514764-122515051 | Common:3; Rare:79 | ||||
| chr3:122564191-122564432 | Common:3; Rare:65 | ||||
| chr3:122564555-122564860 | Rare:84 |