| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:49132985-49133149 | Rare:36; Clinvar:1 | ||||
| chr3:49166294-49166441 | Common:1; Rare:37 | ||||
| chr3:49340026-49340139 | Common:2; Rare:45 | ||||
| chr3:49358253-49358530 | Common:3; Rare:140 | ||||
| chr3:49411839-49412213 | Common:1; Rare:124 | ||||
| chr3:49689451-49689605 | Rare:52 | ||||
| chr3:49856529-49856723 | Common:2; Rare:56 | ||||
| chr3:50350731-50350886 | Common:1; Rare:21 | ||||
| chr3:51385030-51385372 | Common:2; Rare:110 | ||||
| chr3:52154376-52154534 | Common:1; Rare:42 | ||||
| chr3:52239064-52239202 | Common:2; Rare:47 | ||||
| chr3:52455388-52455638 | Common:2; Rare:78 | ||||
| chr3:52685772-52686063 | Common:2; Rare:101 | ||||
| chr3:52705768-52706219 | Common:2; Rare:157 | ||||
| chr3:53130423-53130545 | Common:1; Rare:32; Clinvar (benign):1 |