| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:124876752-124876859 | Common:1; Rare:29 | ||||
| chr11:125592588-125592893 | Common:6; Rare:100 | ||||
| chr11:125625875-125626001 | Rare:43 | ||||
| chr11:125887520-125887727 | Common:2; Rare:61 | ||||
| chr11:126211644-126211804 | Rare:74 | ||||
| chr11:126268814-126269171 | Common:1; Rare:133; Clinvar:1 | ||||
| chr11:126303984-126304098 | Rare:67 | ||||
| chr11:126304239-126304326 | Common:1; Rare:39 | ||||
| chr11:126355526-126355771 | Common:2; Rare:69 | ||||
| chr11:131911346-131911494 | Common:1; Rare:59 | ||||
| chr11:134253310-134253561 | Common:2; Rare:78; Clinvar (benign):1 | ||||
| chr12:389256-389340 | Rare:31 | ||||
| chr12:2812489-2812705 | Common:1; Rare:48 | ||||
| chr12:2877026-2877262 | Rare:70 | ||||
| chr12:4320949-4321247 | Common:4; Rare:112 |