| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:762647-764643 | Common:92; Rare:1717; Clinvar:17; Clinvar (benign):1; Clinvar (pathogenic):13 | ||||
| chr11:776391-777140 | Common:8; Rare:222 | ||||
| chr11:777148-777723 | Common:9; Rare:643 | ||||
| chr11:777911-778378 | Common:4; Rare:206 | ||||
| chr11:796090-796490 | Common:1; Rare:211; Clinvar:5 | ||||
| chr11:797160-797750 | Common:3; Rare:294 | ||||
| chr11:797686-798190 | Common:10; Rare:393 | ||||
| chr11:798210-798520 | Common:4; Rare:162 | ||||
| chr11:805010-805846 | Common:64; Rare:966 | ||||
| chr11:809145-810112 | Common:37; Rare:1368 | ||||
| chr11:810067-811384 | Common:19; Rare:770 | ||||
| chr11:811579-811987 | Common:1; Rare:227 | ||||
| chr11:819250-819941 | Common:15; Rare:731; Clinvar:20; Clinvar (benign):4 | ||||
| chr11:819955-820634 | Common:3; Rare:164 | ||||
| chr11:826863-827263 | Common:2; Rare:168 |