| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:111473836-111474010 | Common:1; Rare:33 | ||||
| chr1:111503671-111503796 | Rare:25 | ||||
| chr1:111619448-111619944 | Common:2; Rare:136 | ||||
| chr1:111739333-111739560 | Common:2; Rare:58 | ||||
| chr1:112395954-112396267 | Common:2; Rare:102 | ||||
| chr1:112619624-112619877 | Common:2; Rare:90 | ||||
| chr1:112674427-112674761 | Common:2; Rare:68 | ||||
| chr1:112707080-112707228 | Rare:50 | ||||
| chr1:112956137-112956521 | Common:5; Rare:154; Clinvar:10; Clinvar (benign):3 | ||||
| chr1:113073085-113073246 | Common:1; Rare:58 | ||||
| chr1:113390163-113390542 | Common:2; Rare:98 | ||||
| chr1:113390725-113391065 | Common:3; Rare:86 | ||||
| chr1:113759448-113759577 | Common:2; Rare:37 | ||||
| chr1:113812251-113812608 | Common:2; Rare:141 | ||||
| chr1:113904742-113905443 | Common:7; Rare:205; Clinvar (benign):2 |