| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:97764489-97764844 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:98522598-98522770 | Rare:41 | ||||
| chr3:98732493-98732512 | Rare:1 | ||||
| chr3:98801213-98801305 | Common:1; Rare:21 | ||||
| chr3:99638478-99638531 | Common:1; Rare:12 | ||||
| chr3:99638545-99638675 | Rare:27 | ||||
| chr3:99817566-99817956 | Rare:121 | ||||
| chr3:100260733-100261028 | Rare:75 | ||||
| chr3:100334642-100334786 | Common:1; Rare:60 | ||||
| chr3:100401375-100401582 | Common:1; Rare:46 | ||||
| chr3:100492277-100492697 | Common:2; Rare:123 | ||||
| chr3:100709179-100709720 | Common:9; Rare:162; Clinvar (benign):1 | ||||
| chr3:100993340-100993603 | Common:3; Rare:54 | ||||
| chr3:101513109-101513336 | Common:8; Rare:48 | ||||
| chr3:101561746-101561979 | Common:2; Rare:87 |