| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57936045-57936385 | Common:3; Rare:82 | ||||
| chr12:64716749-64716976 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:93737786-93737897 | Rare:20 | ||||
| chr12:96241918-96242074 | Rare:33 | ||||
| chr12:103946616-103946941 | Rare:84 | ||||
| chr12:118245895-118246064 | Rare:30 | ||||
| chr12:120291900-120292162 | Common:8; Rare:105 | ||||
| chr12:120293235-120293354 | Common:2; Rare:53 | ||||
| chr12:127060381-127060505 | Common:2; Rare:45 | ||||
| chr12:132939473-132939702 | Common:7; Rare:54 | ||||
| chr13:21297925-21298190 | Common:3; Rare:64 | ||||
| chr13:31846581-31846826 | Common:1; Rare:79 | ||||
| chr13:33015180-33015489 | Common:2; Rare:52 | ||||
| chr13:37008451-37008745 | Rare:61 | ||||
| chr13:37596965-37596991 | Common:1; Rare:2 |