| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:30907904-30908252 | Common:8; Rare:157 | ||||
| chr6:30914174-30914427 | Common:1; Rare:138; Clinvar (benign):5 | ||||
| chr6:31158159-31158628 | Common:16; Rare:227 | ||||
| chr6:31197520-31197800 | Common:16; Rare:137 | ||||
| chr6:31197911-31198143 | Common:7; Rare:72 | ||||
| chr6:31268726-31269638 | Common:95; Rare:287 | ||||
| chr6:31272045-31272287 | Common:32; Rare:68 | ||||
| chr6:31399610-31400140 | Common:22; Rare:150 | ||||
| chr6:31403101-31403766 | Common:25; Rare:250 | ||||
| chr6:31497928-31498163 | Common:21; Rare:77 | ||||
| chr6:31541741-31542425 | Common:18; Rare:397 | ||||
| chr6:31546584-31546949 | Common:6; Rare:125 | ||||
| chr6:31547435-31547733 | Common:3; Rare:112 | ||||
| chr6:31614720-31615540 | Common:5; Rare:166 | ||||
| chr6:31620283-31620847 | Common:2; Rare:308 |