| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:101914858-101915028 | Common:2; Rare:47 | ||||
| chr11:101915121-101915315 | Common:3; Rare:56 | ||||
| chr11:102110211-102110454 | Rare:95 | ||||
| chr11:102317370-102317499 | Rare:32 | ||||
| chr11:102347111-102347298 | Common:2; Rare:62 | ||||
| chr11:102452596-102452943 | Common:2; Rare:111 | ||||
| chr11:103092038-103092259 | Common:1; Rare:68 | ||||
| chr11:105045274-105045613 | Rare:101 | ||||
| chr11:106077326-106077709 | Common:2; Rare:115 | ||||
| chr11:107457800-107457934 | Common:1; Rare:40 | ||||
| chr11:108009096-108009170 | Rare:13 | ||||
| chr11:108009273-108009349 | Rare:38 | ||||
| chr11:108121424-108121621 | Common:4; Rare:72; Clinvar:1; Clinvar (benign):5 | ||||
| chr11:108222597-108223122 | Common:1; Rare:167; Clinvar:7; Clinvar (benign):1 | ||||
| chr11:108223320-108223447 | Rare:35 |