| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:203173565-203173994 | Rare:132 | ||||
| chr1:203177530-203177850 | Common:3; Rare:56 | ||||
| chr1:203178042-203178442 | Common:3; Rare:143 | ||||
| chr1:203222823-203223223 | Common:2; Rare:118; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:203267240-203267610 | Common:2; Rare:96 | ||||
| chr1:203271138-203271321 | Common:2; Rare:24 | ||||
| chr1:203274631-203274746 | Rare:16 | ||||
| chr1:203274923-203275398 | Common:3; Rare:110 | ||||
| chr1:203278274-203278407 | Common:1; Rare:21 | ||||
| chr1:203278508-203278658 | Common:1; Rare:30 | ||||
| chr1:203282528-203282940 | Common:3; Rare:170 | ||||
| chr1:203283090-203283530 | Common:1; Rare:71 | ||||
| chr1:203287213-203287765 | Common:8; Rare:269 | ||||
| chr1:203289451-203289945 | Common:11; Rare:351 | ||||
| chr1:203289990-203290390 | Common:5; Rare:88 |