| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103697196-103697471 | Common:2; Rare:56 | ||||
| chr14:104043265-104043449 | Common:1; Rare:37 | ||||
| chr14:104755435-104755776 | Common:1; Rare:93 | ||||
| chr14:104815498-104815544 | Common:1; Rare:6 | ||||
| chr14:104815947-104816202 | Common:1; Rare:98 | ||||
| chr14:104836659-104836847 | Common:2; Rare:39 | ||||
| chr14:104973216-104973437 | Rare:49 | ||||
| chr14:105027165-105027418 | Common:1; Rare:39 | ||||
| chr14:105033722-105033958 | Common:3; Rare:48 | ||||
| chr14:105092606-105092752 | Rare:18 | ||||
| chr14:105093202-105093463 | Common:1; Rare:76 | ||||
| chr14:105199172-105199341 | Rare:43 | ||||
| chr14:105226647-105227187 | Common:4; Rare:137; Clinvar (pathogenic):1 | ||||
| chr14:105294386-105294583 | Common:1; Rare:42 | ||||
| chr14:105425311-105425439 | Rare:11 |