| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:118754906-118755292 | Common:1; Rare:129 | ||||
| chr10:119080747-119080929 | Rare:70 | ||||
| chr10:119165646-119165776 | Rare:63; Clinvar (benign):3 | ||||
| chr10:119178776-119178940 | Common:3; Rare:67 | ||||
| chr10:119595820-119596096 | Rare:65 | ||||
| chr10:119596448-119596669 | Rare:69 | ||||
| chr10:119596864-119596968 | Common:2; Rare:19 | ||||
| chr10:119596970-119597054 | Rare:23 | ||||
| chr10:119651216-119651397 | Common:5; Rare:72; Clinvar:1; Clinvar (benign):3 | ||||
| chr10:119725753-119726067 | Common:2; Rare:99 | ||||
| chr10:119818625-119818780 | Rare:49 | ||||
| chr10:119892500-119892785 | Common:3; Rare:103 | ||||
| chr10:120851207-120851498 | Common:6; Rare:108 | ||||
| chr10:121927890-121928200 | Common:2; Rare:93 | ||||
| chr10:121928427-121928522 | Rare:29 |