| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:103092028-103092259 | Common:1; Rare:69 | ||||
| chr11:103109275-103109565 | Common:1; Rare:83; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:104164002-104164267 | Common:1; Rare:72 | ||||
| chr11:106077326-106077730 | Common:2; Rare:125 | ||||
| chr11:107457793-107457957 | Common:2; Rare:47 | ||||
| chr11:107591076-107591371 | Rare:99 | ||||
| chr11:108009296-108009361 | Rare:32 | ||||
| chr11:108222585-108223128 | Common:1; Rare:172; Clinvar:8; Clinvar (benign):1 | ||||
| chr11:108664842-108665120 | Common:5; Rare:112 | ||||
| chr11:111766338-111766459 | Common:1; Rare:76 | ||||
| chr11:111878681-111878950 | Common:2; Rare:65 | ||||
| chr11:111879154-111879548 | Common:1; Rare:119 | ||||
| chr11:111913148-111913281 | Rare:41 | ||||
| chr11:111937118-111937217 | Common:5; Rare:39 | ||||
| chr11:112025315-112025482 | Common:1; Rare:40; Clinvar:1; Clinvar (benign):2 |