| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:87037765-87038079 | Common:3; Rare:144 | ||||
| chr11:88337532-88337892 | Common:4; Rare:160; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:90222941-90223170 | Common:2; Rare:89 | ||||
| chr11:93197881-93198039 | Common:2; Rare:53 | ||||
| chr11:93330535-93330746 | Common:2; Rare:64 | ||||
| chr11:93543297-93543682 | Common:5; Rare:97 | ||||
| chr11:93738421-93738705 | Rare:54 | ||||
| chr11:93741381-93741711 | Common:7; Rare:132 | ||||
| chr11:93784027-93784374 | Common:6; Rare:97 | ||||
| chr11:93784421-93784551 | Rare:46 | ||||
| chr11:93784837-93785081 | Common:1; Rare:45 | ||||
| chr11:94128948-94129261 | Common:2; Rare:94 | ||||
| chr11:94493773-94494053 | Common:5; Rare:84; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94543766-94543967 | Common:3; Rare:43 | ||||
| chr11:94973519-94973728 | Rare:68 |