| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:2139270-2139370 | Rare:30 | ||||
| chr11:2377148-2377329 | Common:1; Rare:72 | ||||
| chr11:2400275-2400821 | Common:8; Rare:174 | ||||
| chr11:2444887-2445021 | Rare:41 | ||||
| chr11:2884491-2884707 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:2885744-2885984 | Rare:75; Clinvar:1 | ||||
| chr11:2902017-2902385 | Common:1; Rare:82 | ||||
| chr11:2903407-2903839 | Common:11; Rare:183 | ||||
| chr11:2929415-2929568 | Rare:28 | ||||
| chr11:2992229-2992586 | Common:2; Rare:145 | ||||
| chr11:3057359-3057640 | Rare:100 | ||||
| chr11:3126609-3126797 | Common:2; Rare:43 | ||||
| chr11:3165237-3165411 | Common:1; Rare:54 | ||||
| chr11:3379059-3379405 | Common:4; Rare:90 | ||||
| chr11:3642107-3642265 | Common:8; Rare:69 |