| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:179954675-179954828 | Common:1; Rare:57 | ||||
| chr1:180154570-180154937 | Common:5; Rare:181 | ||||
| chr1:180502460-180502729 | Common:2; Rare:191 | ||||
| chr1:180502807-180503056 | Rare:123 | ||||
| chr1:181022770-181023262 | Common:26; Rare:292 | ||||
| chr1:182391130-182391710 | Common:3; Rare:196; Clinvar (benign):1 | ||||
| chr1:182391733-182392028 | Common:6; Rare:177; Clinvar:8; Clinvar (benign):6 | ||||
| chr1:182839088-182839401 | Common:2; Rare:228 | ||||
| chr1:182839460-182839840 | Common:5; Rare:248 | ||||
| chr1:183022994-183023646 | Common:11; Rare:236 | ||||
| chr1:183471610-183472130 | Common:3; Rare:180 | ||||
| chr1:183472253-183472524 | Common:4; Rare:183 | ||||
| chr1:183472910-183473590 | Common:5; Rare:146 | ||||
| chr1:183635566-183636191 | Common:10; Rare:295 | ||||
| chr1:183805007-183805240 | Rare:95 |