| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:244461256-244461334 | Common:2; Rare:19 | ||||
| chr1:244835549-244835723 | Common:2; Rare:75; Clinvar (benign):4 | ||||
| chr1:244863931-244864349 | Common:1; Rare:125; Clinvar:3; Clinvar (benign):6 | ||||
| chr1:244864398-244864724 | Common:1; Rare:133 | ||||
| chr1:244970008-244970433 | Common:5; Rare:181 | ||||
| chr1:246507089-246507140 | Rare:13 | ||||
| chr1:246507229-246507332 | Rare:43 | ||||
| chr1:246566218-246566584 | Common:1; Rare:121 | ||||
| chr1:246724212-246724508 | Common:2; Rare:106 | ||||
| chr1:248825852-248825983 | Common:2; Rare:35 | ||||
| chr1:248826454-248826764 | Common:3; Rare:60 | ||||
| chr1:248858919-248859040 | Rare:47 | ||||
| chr10:134622-134816 | Rare:50 | ||||
| chr10:135371-135540 | Rare:46 | ||||
| chr10:650326-650368 | Rare:12 |