| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111918451-111919075 | Common:4; Rare:272 | ||||
| chr11:111923470-111924040 | Common:4; Rare:119 | ||||
| chr11:111926810-111927315 | Common:24; Rare:193 | ||||
| chr11:111936720-111937560 | Common:20; Rare:341 | ||||
| chr11:112024938-112025223 | Rare:125; Clinvar:6 | ||||
| chr11:112025313-112025616 | Common:4; Rare:131; Clinvar:2; Clinvar (benign):7 | ||||
| chr11:112073995-112074363 | Common:1; Rare:119 | ||||
| chr11:112086707-112086928 | Rare:182; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr11:112226194-112226696 | Common:1; Rare:232; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:113314408-113314617 | Rare:75 | ||||
| chr11:113773664-113773856 | Common:1; Rare:59 | ||||
| chr11:113875493-113875791 | Common:8; Rare:222 | ||||
| chr11:114400412-114400755 | Common:4; Rare:266 | ||||
| chr11:114439348-114439542 | Common:1; Rare:64 | ||||
| chr11:115504361-115504673 | Common:3; Rare:173 |