| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:51026130-51026673 | Common:14; Rare:402; Clinvar:8; Clinvar (benign):6 | ||||
| chr12:51028188-51028553 | Common:1; Rare:68 | ||||
| chr12:51047790-51048441 | Common:11; Rare:432 | ||||
| chr12:51082500-51083070 | Common:2; Rare:131 | ||||
| chr12:51083390-51083808 | Common:1; Rare:261 | ||||
| chr12:51217734-51218280 | Common:7; Rare:198 | ||||
| chr12:51238462-51238946 | Common:26; Rare:401 | ||||
| chr12:51239004-51239365 | Common:9; Rare:252 | ||||
| chr12:51269731-51270130 | Common:6; Rare:329 | ||||
| chr12:51270117-51270461 | Common:12; Rare:245 | ||||
| chr12:51383450-51383810 | Common:1; Rare:61 | ||||
| chr12:51390975-51391562 | Common:6; Rare:240 | ||||
| chr12:51391537-51391944 | Common:5; Rare:194 | ||||
| chr12:51424451-51424942 | Common:4; Rare:155 | ||||
| chr12:51590710-51591250 | Common:3; Rare:249 |