| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:6320485-6320621 | Common:2; Rare:47 | ||||
| chr11:6390206-6390506 | Common:4; Rare:166 | ||||
| chr11:6473855-6474072 | Rare:134 | ||||
| chr11:6481248-6481585 | Common:10; Rare:269 | ||||
| chr11:6603529-6604064 | Common:9; Rare:255; Clinvar (benign):6 | ||||
| chr11:6611959-6612332 | Common:4; Rare:195 | ||||
| chr11:6619371-6619578 | Common:3; Rare:66; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr11:6683126-6683656 | Common:12; Rare:344 | ||||
| chr11:7513638-7513782 | Common:1; Rare:44 | ||||
| chr11:7573715-7574004 | Common:1; Rare:57 | ||||
| chr11:8594120-8594580 | Common:3; Rare:195 | ||||
| chr11:8682604-8683101 | Common:5; Rare:403 | ||||
| chr11:8870267-8870630 | Common:10; Rare:146 | ||||
| chr11:8870810-8871290 | Common:2; Rare:136 | ||||
| chr11:8871359-8871490 | Rare:27 |