| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:37433116-37433294 | Common:3; Rare:53 | ||||
| chr6:38639860-38639986 | Rare:35 | ||||
| chr6:41921079-41921229 | Common:1; Rare:40 | ||||
| chr6:42217823-42217967 | Common:4; Rare:45 | ||||
| chr6:42879613-42879943 | Rare:96 | ||||
| chr6:42929234-42929565 | Common:3; Rare:94 | ||||
| chr6:42984307-42984635 | Rare:86 | ||||
| chr6:43013793-43014323 | Common:2; Rare:136 | ||||
| chr6:43516786-43517141 | Common:6; Rare:130; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:43575942-43576188 | Rare:96; Clinvar:4 | ||||
| chr6:43687768-43687828 | Common:1; Rare:23 | ||||
| chr6:43770071-43770254 | Common:3; Rare:54 | ||||
| chr6:44127351-44127634 | Common:4; Rare:80 | ||||
| chr6:44223441-44223606 | Common:1; Rare:47 | ||||
| chr6:44387445-44387753 | Common:4; Rare:82 |