| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196739693-196739994 | Rare:99 | ||||
| chr3:196867575-196867967 | Rare:113 | ||||
| chr3:196942373-196942725 | Common:1; Rare:158 | ||||
| chr3:196968694-196969494 | Common:7; Rare:438 | ||||
| chr3:197029780-197030050 | Common:2; Rare:76 | ||||
| chr3:197297981-197298316 | Common:1; Rare:127 | ||||
| chr3:197298561-197298809 | Rare:75 | ||||
| chr3:197554700-197555300 | Common:5; Rare:156 | ||||
| chr3:197736851-197737232 | Common:3; Rare:122 | ||||
| chr3:197749661-197749962 | Common:1; Rare:99 | ||||
| chr3:197750178-197750743 | Common:8; Rare:220 | ||||
| chr3:197791094-197791330 | Common:3; Rare:92 | ||||
| chr3:197949828-197950269 | Common:4; Rare:125; Clinvar (benign):2 | ||||
| chr3:197959982-197960287 | Common:1; Rare:117 | ||||
| chr3:197960722-197960970 | Common:1; Rare:43 |