| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:101583973-101584123 | Rare:38 | ||||
| chr11:102317234-102317563 | Rare:65 | ||||
| chr11:102347100-102347458 | Common:4; Rare:101 | ||||
| chr11:102452526-102452949 | Common:2; Rare:138 | ||||
| chr11:103092034-103092261 | Common:1; Rare:70 | ||||
| chr11:103109346-103109576 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:106022178-106022559 | Common:3; Rare:111 | ||||
| chr11:106077317-106077711 | Common:2; Rare:119 | ||||
| chr11:107457738-107457940 | Common:2; Rare:74 | ||||
| chr11:107928119-107928536 | Common:4; Rare:101 | ||||
| chr11:108008775-108008995 | Rare:63 | ||||
| chr11:108009113-108009187 | Rare:17 | ||||
| chr11:108009190-108009283 | Rare:34 | ||||
| chr11:108009284-108009369 | Rare:39 | ||||
| chr11:108121404-108121621 | Common:5; Rare:75; Clinvar:1; Clinvar (benign):5 |