| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111937082-111937217 | Common:5; Rare:45 | ||||
| chr11:112025293-112025486 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:112073995-112074349 | Common:1; Rare:72 | ||||
| chr11:112086700-112086905 | Rare:89; Clinvar:1 | ||||
| chr11:112226140-112226847 | Common:2; Rare:227; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:112961307-112961654 | Common:4; Rare:170 | ||||
| chr11:113314448-113314602 | Rare:54 | ||||
| chr11:113875497-113875775 | Common:4; Rare:103 | ||||
| chr11:114059385-114059764 | Rare:82 | ||||
| chr11:114400456-114400753 | Common:2; Rare:118 | ||||
| chr11:115504362-115504673 | Common:2; Rare:97 | ||||
| chr11:117144188-117144354 | Common:2; Rare:85 | ||||
| chr11:117232043-117232191 | Rare:38 | ||||
| chr11:117232525-117232714 | Common:2; Rare:66 | ||||
| chr11:117316323-117316432 | Common:1; Rare:30 |