| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:42943240-42943610 | Common:5; Rare:158; Clinvar:4; Clinvar (benign):9 | ||||
| chr1:42957930-42958360 | Common:12; Rare:246 | ||||
| chr1:42958756-42959082 | Common:8; Rare:160; Clinvar:12; Clinvar (benign):8 | ||||
| chr1:43172215-43172359 | Common:2; Rare:125 | ||||
| chr1:43172470-43172750 | Common:12; Rare:131 | ||||
| chr1:43358650-43359102 | Common:14; Rare:262 | ||||
| chr1:43367476-43367871 | Common:4; Rare:134 | ||||
| chr1:43367936-43368243 | Rare:148 | ||||
| chr1:43389726-43389990 | Common:8; Rare:202; Clinvar:2 | ||||
| chr1:43530773-43531065 | Common:6; Rare:170 | ||||
| chr1:43538030-43538720 | Common:2; Rare:181 | ||||
| chr1:43649830-43650190 | Rare:163 | ||||
| chr1:43650302-43650571 | Common:1; Rare:128 | ||||
| chr1:43707307-43707571 | Common:4; Rare:136 | ||||
| chr1:43707610-43707920 | Common:2; Rare:186 |