| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:111988720-111989040 | Common:1; Rare:55; Clinvar (benign):1 | ||||
| chr1:111989160-111990040 | Common:6; Rare:401 | ||||
| chr1:112395962-112396298 | Common:5; Rare:269 | ||||
| chr1:112466080-112466410 | Common:4; Rare:73 | ||||
| chr1:112508530-112509120 | Common:5; Rare:202 | ||||
| chr1:112618632-112618898 | Common:2; Rare:90 | ||||
| chr1:112618880-112619313 | Rare:286 | ||||
| chr1:112619447-112619917 | Common:7; Rare:297 | ||||
| chr1:112674397-112675245 | Common:6; Rare:342 | ||||
| chr1:112707002-112707287 | Rare:218 | ||||
| chr1:112707253-112707670 | Common:2; Rare:194 | ||||
| chr1:112715149-112715630 | Common:2; Rare:365 | ||||
| chr1:112956131-112956490 | Common:14; Rare:337; Clinvar:25; Clinvar (benign):9 | ||||
| chr1:113073039-113073451 | Common:3; Rare:298 | ||||
| chr1:113073500-113073950 | Common:3; Rare:244 |