| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:112446892-112447284 | Common:3; Rare:97 | ||||
| chr10:113854392-113854627 | Rare:46 | ||||
| chr10:113854631-113854864 | Common:1; Rare:59 | ||||
| chr10:118046684-118047008 | Common:4; Rare:105 | ||||
| chr10:118754930-118755292 | Common:1; Rare:119 | ||||
| chr10:119080772-119080927 | Rare:62 | ||||
| chr10:119178765-119178862 | Common:1; Rare:44 | ||||
| chr10:119596959-119597047 | Rare:25 | ||||
| chr10:119892504-119892772 | Common:3; Rare:98 | ||||
| chr10:120851200-120851406 | Common:4; Rare:70 | ||||
| chr10:121927945-121928094 | Common:1; Rare:56 | ||||
| chr10:121928433-121928536 | Rare:26 | ||||
| chr10:122954197-122954496 | Rare:109 | ||||
| chr10:122980366-122980435 | Common:1; Rare:11 | ||||
| chr10:123008791-123009021 | Common:5; Rare:62; Clinvar:4; Clinvar (benign):5 |