| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:112619064-112619212 | Rare:53 | ||||
| chr1:112619642-112619877 | Common:2; Rare:84 | ||||
| chr1:112674611-112674893 | Common:1; Rare:59 | ||||
| chr1:112707080-112707221 | Rare:47 | ||||
| chr1:112956061-112956659 | Common:6; Rare:184; Clinvar:12; Clinvar (benign):3 | ||||
| chr1:113073085-113073238 | Common:1; Rare:55 | ||||
| chr1:113390205-113390532 | Common:1; Rare:82 | ||||
| chr1:113812264-113812608 | Common:2; Rare:134 | ||||
| chr1:113904775-113905432 | Common:7; Rare:190; Clinvar (benign):2 | ||||
| chr1:114581572-114581841 | Common:1; Rare:117 | ||||
| chr1:114669991-114670255 | Common:1; Rare:83 | ||||
| chr1:114716665-114716891 | Common:1; Rare:96; Clinvar:5; Clinvar (benign):3 | ||||
| chr1:114757923-114758103 | Common:3; Rare:58 | ||||
| chr1:114780539-114780806 | Common:1; Rare:102 | ||||
| chr1:115641810-115642043 | Common:3; Rare:78; Clinvar:1; Clinvar (benign):2 |