| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:105854202-105854561 | Common:1; Rare:129 | ||||
| chr14:105854723-105854925 | Rare:52 | ||||
| chr14:105854910-105855306 | Common:4; Rare:111 | ||||
| chr14:105855473-105856125 | Common:9; Rare:351; Clinvar (benign):2 | ||||
| chr14:105861031-105861580 | Common:4; Rare:440 | ||||
| chr14:105861913-105862361 | Common:6; Rare:245 | ||||
| chr14:105862456-105862790 | Common:7; Rare:258 | ||||
| chr14:105863172-105863530 | Common:12; Rare:716 | ||||
| chr14:105863900-105864420 | Common:11; Rare:805 | ||||
| chr14:105886811-105886992 | Rare:38 | ||||
| chr14:105887160-105887324 | Common:1; Rare:33 | ||||
| chr14:105894396-105894796 | Common:6; Rare:300 | ||||
| chr14:105902687-105902864 | Common:16; Rare:131 | ||||
| chr14:105903943-105904214 | Common:7; Rare:111 | ||||
| chr14:105905353-105905701 | Common:2; Rare:179 |