| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3840898-3841085 | Rare:79 | ||||
| chr11:3855580-3855672 | Common:2; Rare:21 | ||||
| chr11:3855948-3855962 | Rare:3 | ||||
| chr11:4094735-4094840 | Common:1; Rare:32 | ||||
| chr11:4608171-4608405 | Common:1; Rare:64 | ||||
| chr11:5624880-5625034 | Rare:25 | ||||
| chr11:6390241-6390498 | Common:2; Rare:72 | ||||
| chr11:6419061-6419181 | Common:2; Rare:27 | ||||
| chr11:6481285-6481527 | Common:4; Rare:98 | ||||
| chr11:6603539-6603838 | Common:4; Rare:89; Clinvar (benign):3 | ||||
| chr11:6612205-6612342 | Common:2; Rare:42 | ||||
| chr11:6614929-6615233 | Common:1; Rare:82; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr11:6619377-6619562 | Common:3; Rare:60; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr11:6683294-6683553 | Common:5; Rare:101 | ||||
| chr11:7513604-7513979 | Common:6; Rare:115 |