| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:35921057-35921261 | Common:1; Rare:85 | ||||
| chr6:36442915-36443077 | Common:2; Rare:64 | ||||
| chr6:36874779-36874882 | Rare:41 | ||||
| chr6:37257606-37257783 | Rare:42 | ||||
| chr6:38639811-38640027 | Rare:55 | ||||
| chr6:39229471-39229584 | Common:2; Rare:46 | ||||
| chr6:39934449-39934587 | Common:1; Rare:74 | ||||
| chr6:41921115-41921223 | Rare:27 | ||||
| chr6:42746069-42746348 | Rare:79 | ||||
| chr6:42929226-42929562 | Common:3; Rare:94 | ||||
| chr6:42984295-42984609 | Rare:76 | ||||
| chr6:43013878-43014287 | Common:2; Rare:90 | ||||
| chr6:43516887-43517123 | Common:4; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575983-43576197 | Rare:75; Clinvar:4 | ||||
| chr6:43687757-43687860 | Common:1; Rare:42 |