| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:133244226-133244357 | Common:2; Rare:32; Clinvar:1 | ||||
| chr8:134713010-134713151 | Common:1; Rare:46 | ||||
| chr8:140511201-140511509 | Common:3; Rare:115 | ||||
| chr8:141001142-141001418 | Common:2; Rare:92 | ||||
| chr8:142669945-142670300 | Common:9; Rare:126 | ||||
| chr8:142700370-142700501 | Common:4; Rare:58 | ||||
| chr8:142742340-142742517 | Common:3; Rare:47; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr8:142786458-142786688 | Common:4; Rare:56 | ||||
| chr8:143018406-143018575 | Common:1; Rare:48 | ||||
| chr8:143213022-143213262 | Rare:64 | ||||
| chr8:143267143-143267473 | Common:1; Rare:127 | ||||
| chr8:143269835-143269885 | Rare:6 | ||||
| chr8:143541426-143541636 | Common:2; Rare:70 | ||||
| chr8:143558267-143558354 | Common:1; Rare:33 | ||||
| chr8:143572734-143572855 | Rare:41 |