| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143936057-143936159 | Common:2; Rare:17 | ||||
| chr8:143936264-143936662 | Common:4; Rare:91 | ||||
| chr8:143936762-143937006 | Rare:61 | ||||
| chr8:143937870-143938316 | Common:3; Rare:139; Clinvar:4; Clinvar (benign):4 | ||||
| chr8:143938489-143938695 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:144262126-144262497 | Rare:67 | ||||
| chr8:144973880-144974039 | Rare:30 | ||||
| chr8:144975774-144975840 | Common:1; Rare:9 | ||||
| chr8:144975881-144975984 | Common:1; Rare:22 | ||||
| chr8:144976368-144976391 | Rare:5 | ||||
| chr8:144976664-144976982 | Rare:95 | ||||
| chr8:144977587-144977721 | Rare:36 | ||||
| chr8:144994545-144994557 | Rare:3 | ||||
| chr8:144998773-144998887 | Rare:13 | ||||
| chr8:145002835-145003041 | Common:2; Rare:71 |