| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:6490690-6491205 | Common:1; Rare:195 | ||||
| chr1:6497340-6497630 | Common:2; Rare:88 | ||||
| chr1:6497650-6498000 | Common:1; Rare:63 | ||||
| chr1:6554477-6554680 | Common:5; Rare:70 | ||||
| chr1:6579821-6580111 | Common:4; Rare:93 | ||||
| chr1:6602857-6603139 | Common:3; Rare:95 | ||||
| chr1:6603536-6603678 | Common:1; Rare:28 | ||||
| chr1:6613448-6613778 | Common:2; Rare:116 | ||||
| chr1:6614244-6614663 | Common:1; Rare:214 | ||||
| chr1:6625051-6625201 | Rare:62 | ||||
| chr1:6701712-6702000 | Rare:83 | ||||
| chr1:6785452-6785570 | Common:2; Rare:39 | ||||
| chr1:7771098-7771332 | Common:4; Rare:85 | ||||
| chr1:7783670-7784120 | Common:5; Rare:118 | ||||
| chr1:7961410-7961738 | Common:3; Rare:116; Clinvar:2; Clinvar (benign):2 |