| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:133393888-133394212 | Common:2; Rare:117 | ||||
| chr11:207361-207511 | Common:4; Rare:60 | ||||
| chr11:208688-208843 | Rare:61 | ||||
| chr11:236909-237047 | Common:1; Rare:55 | ||||
| chr11:615946-616030 | Rare:25 | ||||
| chr11:777465-777599 | Common:1; Rare:59 | ||||
| chr11:809833-810037 | Common:2; Rare:94 | ||||
| chr11:832881-833002 | Common:7; Rare:41 | ||||
| chr11:842467-842895 | Common:7; Rare:178 | ||||
| chr11:1309594-1309851 | Common:2; Rare:110 | ||||
| chr11:3379111-3379309 | Common:2; Rare:50 | ||||
| chr11:6481302-6481524 | Common:4; Rare:88 | ||||
| chr11:6603550-6603822 | Common:4; Rare:83; Clinvar (benign):3 | ||||
| chr11:7020327-7020600 | Common:1; Rare:90 | ||||
| chr11:8682648-8682816 | Common:2; Rare:74 |