| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119018383-119018459 | Common:2; Rare:21 | ||||
| chr11:124673715-124673927 | Common:4; Rare:64 | ||||
| chr11:126268841-126269117 | Common:1; Rare:96; Clinvar:1 | ||||
| chr12:42326092-42326171 | Rare:22 | ||||
| chr12:120201097-120201348 | Common:2; Rare:77 | ||||
| chr12:123633640-123633825 | Common:1; Rare:77; Clinvar:8; Clinvar (benign):1 | ||||
| chr13:110307155-110307296 | Rare:47 | ||||
| chr14:24232337-24232465 | Common:6; Rare:28 | ||||
| chr14:49620596-49620815 | Common:2; Rare:76; Clinvar:1 | ||||
| chr14:77708005-77708103 | Rare:47 | ||||
| chr14:100376310-100376476 | Common:2; Rare:56 | ||||
| chr15:40039126-40039264 | Rare:56 | ||||
| chr15:90233924-90234209 | Common:4; Rare:79 | ||||
| chr16:2047825-2047994 | Rare:65 | ||||
| chr16:8797628-8797870 | Rare:92; Clinvar:2; Clinvar (benign):2 |