| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:183236351-183236598 | Common:2; Rare:63; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr1:183272354-183272684 | Common:5; Rare:56 | ||||
| chr1:183281935-183282046 | Common:1; Rare:19 | ||||
| chr1:183427530-183427831 | Common:2; Rare:50 | ||||
| chr1:183470203-183470513 | Common:3; Rare:65 | ||||
| chr1:183471047-183471340 | Rare:49 | ||||
| chr1:183697098-183697156 | Rare:5 | ||||
| chr1:183698016-183698299 | Common:3; Rare:43 | ||||
| chr1:183699593-183700136 | Common:2; Rare:80 | ||||
| chr1:183719337-183719435 | Rare:16 | ||||
| chr1:183719443-183719607 | Common:1; Rare:28 | ||||
| chr1:183734909-183734928 | Rare:4 | ||||
| chr1:183735253-183735448 | Common:1; Rare:32 | ||||
| chr1:183996550-183996713 | Common:1; Rare:29 | ||||
| chr1:184036434-184036598 | Common:1; Rare:36 |