| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:87765919-87766028 | Rare:44 | ||||
| chr16:88570122-88570414 | Common:2; Rare:108 | ||||
| chr16:88663076-88663362 | Common:7; Rare:116 | ||||
| chr16:88856932-88857153 | Common:4; Rare:97; Clinvar (benign):2 | ||||
| chr16:89217632-89217738 | Common:1; Rare:47 | ||||
| chr16:89508305-89508452 | Common:1; Rare:81; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:89560490-89560717 | Rare:104 | ||||
| chr16:89657660-89658047 | Common:3; Rare:204 | ||||
| chr16:89686540-89686707 | Common:7; Rare:73 | ||||
| chr16:89923110-89923357 | Common:1; Rare:92 | ||||
| chr16:89948560-89948809 | Common:3; Rare:75 | ||||
| chr16:89972478-89972627 | Common:1; Rare:55 | ||||
| chr16:90022581-90022709 | Rare:51 | ||||
| chr17:714785-714953 | Common:3; Rare:58 | ||||
| chr17:732324-732611 | Common:2; Rare:99 |