| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201642622-201642790 | Common:1; Rare:76; Clinvar (benign):1 | ||||
| chr2:201643389-201643504 | Common:2; Rare:38; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:201780884-201781003 | Common:2; Rare:34; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:202238443-202238644 | Rare:71; Clinvar:1 | ||||
| chr2:202265685-202265819 | Rare:54 | ||||
| chr2:202377071-202377384 | Common:2; Rare:66; Clinvar (benign):4 | ||||
| chr2:202634795-202635026 | Common:5; Rare:86 | ||||
| chr2:202911602-202911729 | Rare:24 | ||||
| chr2:202912102-202912554 | Common:4; Rare:136 | ||||
| chr2:203014622-203015004 | Common:1; Rare:120 | ||||
| chr2:203238864-203239101 | Common:2; Rare:93 | ||||
| chr2:203239201-203239394 | Rare:66 | ||||
| chr2:203328178-203328544 | Common:2; Rare:125 | ||||
| chr2:203328888-203328914 | Rare:7 | ||||
| chr2:203535086-203535557 | Common:3; Rare:167 |