| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95924078-95924158 | Rare:31 | ||||
| chr11:96389866-96390043 | Common:1; Rare:70 | ||||
| chr11:99020598-99021052 | Rare:124 | ||||
| chr11:101914813-101915066 | Common:3; Rare:67 | ||||
| chr11:101915106-101915330 | Common:3; Rare:65 | ||||
| chr11:102047140-102047468 | Common:1; Rare:76 | ||||
| chr11:102110228-102110449 | Rare:88 | ||||
| chr11:102347131-102347312 | Common:2; Rare:65 | ||||
| chr11:102452665-102452905 | Rare:77 | ||||
| chr11:103092078-103092259 | Common:1; Rare:61 | ||||
| chr11:103109303-103109570 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:105609907-105610136 | Common:1; Rare:47 | ||||
| chr11:105610828-105610986 | Common:1; Rare:50 | ||||
| chr11:106022180-106022573 | Common:3; Rare:113 | ||||
| chr11:106077311-106077730 | Common:2; Rare:130 |