| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119597308-119597418 | Common:3; Rare:22 | ||||
| chr10:119651210-119651392 | Common:4; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr10:119725767-119725826 | Rare:23 | ||||
| chr10:119726162-119726240 | Rare:25 | ||||
| chr10:119818486-119818850 | Rare:123 | ||||
| chr10:119892540-119892789 | Common:3; Rare:93 | ||||
| chr10:120851146-120851445 | Common:5; Rare:108 | ||||
| chr10:121927890-121928197 | Common:2; Rare:91 | ||||
| chr10:121928429-121928555 | Rare:34 | ||||
| chr10:122112856-122113096 | Common:3; Rare:75 | ||||
| chr10:122374459-122374784 | Common:1; Rare:105 | ||||
| chr10:122375130-122375231 | Common:1; Rare:38 | ||||
| chr10:122699775-122699966 | Common:1; Rare:50 | ||||
| chr10:122879501-122879714 | Common:3; Rare:56 | ||||
| chr10:122954174-122954598 | Common:2; Rare:131 |