| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:92298945-92299076 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:92785066-92785136 | Common:1; Rare:36 | ||||
| chr1:93079064-93079280 | Common:3; Rare:97 | ||||
| chr1:93180362-93180744 | Common:2; Rare:166 | ||||
| chr1:93345772-93345904 | Common:4; Rare:54 | ||||
| chr1:93879144-93879274 | Common:1; Rare:44 | ||||
| chr1:94418088-94418464 | Common:3; Rare:133 | ||||
| chr1:95072884-95073050 | Common:1; Rare:62 | ||||
| chr1:95233950-95234231 | Common:5; Rare:82 | ||||
| chr1:98661596-98661869 | Common:2; Rare:98 | ||||
| chr1:99850336-99850668 | Rare:77; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:99969904-99970080 | Rare:44 | ||||
| chr1:100038007-100038122 | Rare:47 | ||||
| chr1:100132911-100133202 | Common:2; Rare:104 | ||||
| chr1:100266109-100266332 | Common:2; Rare:81 |