| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:119101752-119102255 | Rare:128; Clinvar:4 | ||||
| chr11:119102399-119102504 | Common:4; Rare:17 | ||||
| chr11:119102726-119102827 | Rare:13 | ||||
| chr11:119106874-119106929 | Rare:6 | ||||
| chr11:119107060-119107444 | Common:3; Rare:99 | ||||
| chr11:119108360-119108376 | Rare:3 | ||||
| chr11:119121170-119121229 | Rare:13 | ||||
| chr11:119121237-119121691 | Common:1; Rare:119 | ||||
| chr11:119168667-119168874 | Rare:52 | ||||
| chr11:119168936-119169201 | Rare:55 | ||||
| chr11:119169291-119169369 | Rare:18 | ||||
| chr11:119205806-119206110 | Common:2; Rare:93 | ||||
| chr11:119206128-119206438 | Common:5; Rare:126; Clinvar:8; Clinvar (benign):6 | ||||
| chr11:119317103-119317288 | Rare:62 | ||||
| chr11:119318821-119318963 | Common:1; Rare:29 |