| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100837374-100837582 | Common:1; Rare:55 | ||||
| chr7:100890278-100890355 | Rare:17 | ||||
| chr7:101122321-101122450 | Common:3; Rare:19 | ||||
| chr7:101138608-101138733 | Common:1; Rare:31; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:101163642-101163780 | Rare:52 | ||||
| chr7:101174040-101174135 | Rare:23 | ||||
| chr7:101688349-101688498 | Common:3; Rare:41 | ||||
| chr7:101741019-101741090 | Common:1; Rare:5 | ||||
| chr7:101816669-101816756 | Rare:14 | ||||
| chr7:101981717-101981732 | Rare:4 | ||||
| chr7:101991056-101991315 | Common:1; Rare:55 | ||||
| chr7:102062098-102062294 | Common:1; Rare:40 | ||||
| chr7:102287441-102287714 | Rare:62 | ||||
| chr7:102287910-102287953 | Rare:8 | ||||
| chr7:102288961-102289006 | Common:1; Rare:9 |