| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:102452529-102452943 | Common:2; Rare:136 | ||||
| chr11:103092038-103092262 | Common:1; Rare:71 | ||||
| chr11:103109307-103109572 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:105609972-105610370 | Common:1; Rare:84 | ||||
| chr11:105610529-105610561 | Rare:10 | ||||
| chr11:105610591-105610801 | Rare:43 | ||||
| chr11:106022175-106022561 | Common:3; Rare:114 | ||||
| chr11:106077283-106077734 | Common:2; Rare:143 | ||||
| chr11:107457749-107457946 | Common:2; Rare:67 | ||||
| chr11:107565699-107565803 | Rare:30 | ||||
| chr11:107591072-107591317 | Rare:84 | ||||
| chr11:107928119-107928611 | Common:5; Rare:124 | ||||
| chr11:108009273-108009361 | Rare:42 | ||||
| chr11:108121384-108121621 | Common:5; Rare:79; Clinvar:1; Clinvar (benign):5 | ||||
| chr11:108222568-108223424 | Common:1; Rare:259; Clinvar:10; Clinvar (benign):4 |