| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:114757877-114758091 | Common:4; Rare:111 | ||||
| chr1:114780541-114780805 | Common:2; Rare:188 | ||||
| chr1:115641730-115642048 | Common:7; Rare:185; Clinvar:2; Clinvar (benign):4 | ||||
| chr1:115976060-115976540 | Common:2; Rare:241 | ||||
| chr1:116373117-116373525 | Common:4; Rare:238 | ||||
| chr1:116570975-116571189 | Common:2; Rare:63 | ||||
| chr1:117060038-117060363 | Common:13; Rare:171 | ||||
| chr1:117367273-117367576 | Common:10; Rare:193 | ||||
| chr1:117929543-117929884 | Common:8; Rare:192 | ||||
| chr1:119140596-119140782 | Common:2; Rare:120; Clinvar (pathogenic):1 | ||||
| chr1:119648109-119648350 | Common:6; Rare:162 | ||||
| chr1:120176315-120176556 | Rare:99 | ||||
| chr1:145093680-145093921 | Common:1; Rare:37 | ||||
| chr1:145706820-145707226 | Common:2; Rare:126 | ||||
| chr1:145707329-145707448 | Common:2; Rare:28 |