| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:9474361-9474665 | Common:20; Rare:239 | ||||
| chr2:9474709-9474912 | Common:2; Rare:52 | ||||
| chr2:9474941-9476441 | Common:20; Rare:686 | ||||
| chr2:9555588-9556264 | Common:9; Rare:499 | ||||
| chr2:9630280-9630760 | Common:10; Rare:351 | ||||
| chr2:9630740-9630872 | Common:1; Rare:54 | ||||
| chr2:9630892-9631316 | Common:3; Rare:182 | ||||
| chr2:9843179-9843876 | Common:35; Rare:520 | ||||
| chr2:9951369-9952017 | Common:19; Rare:537 | ||||
| chr2:10043276-10043713 | Common:11; Rare:423; Clinvar:7; Clinvar (benign):2 | ||||
| chr2:10043836-10044480 | Common:30; Rare:555 | ||||
| chr2:10122140-10122470 | Common:1; Rare:166 | ||||
| chr2:10122480-10122846 | Common:16; Rare:385 | ||||
| chr2:10302409-10303024 | Common:18; Rare:420 | ||||
| chr2:10303985-10304385 | Common:4; Rare:128 |