| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42879577-42879949 | Rare:110 | ||||
| chr6:42929120-42929181 | Rare:16 | ||||
| chr6:42929209-42929406 | Common:3; Rare:46 | ||||
| chr6:42929409-42929573 | Common:1; Rare:60 | ||||
| chr6:42984277-42984649 | Rare:102 | ||||
| chr6:43013838-43014323 | Common:2; Rare:119 | ||||
| chr6:43053780-43054073 | Common:1; Rare:81; Clinvar:5 | ||||
| chr6:43059811-43059890 | Rare:26 | ||||
| chr6:43076173-43076479 | Rare:100 | ||||
| chr6:43427467-43427576 | Rare:34 | ||||
| chr6:43456052-43456312 | Rare:55 | ||||
| chr6:43516850-43517167 | Common:5; Rare:122; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575945-43576240 | Common:1; Rare:121; Clinvar:8 | ||||
| chr6:43625523-43625803 | Rare:73 | ||||
| chr6:43629120-43629523 | Common:2; Rare:119 |