| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:172427411-172427741 | Common:8; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:172427911-172428076 | Common:5; Rare:49; Clinvar (benign):2 | ||||
| chr2:172555526-172555693 | Rare:39 | ||||
| chr2:172555775-172556160 | Common:4; Rare:157 | ||||
| chr2:172556451-172556577 | Common:1; Rare:32 | ||||
| chr2:172556606-172556648 | Rare:11 | ||||
| chr2:173075428-173075711 | Common:5; Rare:67 | ||||
| chr2:173075746-173076135 | Common:3; Rare:100 | ||||
| chr2:173076225-173076372 | Common:3; Rare:46 | ||||
| chr2:173076412-173076449 | Rare:6 | ||||
| chr2:173354118-173354372 | Common:1; Rare:46 | ||||
| chr2:173354484-173354955 | Common:1; Rare:141 | ||||
| chr2:173355211-173355244 | Rare:11 | ||||
| chr2:173355384-173355575 | Common:5; Rare:46 | ||||
| chr2:173963354-173963622 | Common:2; Rare:81 |