| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:158819316-158819485 | Common:2; Rare:65 | ||||
| chr6:158999722-158999975 | Common:1; Rare:110; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:159000135-159000305 | Common:1; Rare:43 | ||||
| chr6:159693144-159693609 | Common:6; Rare:143 | ||||
| chr6:159726870-159727033 | Common:1; Rare:81 | ||||
| chr6:159727057-159727181 | Rare:41 | ||||
| chr6:159727322-159727624 | Common:5; Rare:128 | ||||
| chr6:159761853-159762101 | Common:4; Rare:125 | ||||
| chr6:159762310-159762466 | Common:1; Rare:41 | ||||
| chr6:159789514-159790033 | Common:5; Rare:172 | ||||
| chr6:159790257-159790516 | Common:7; Rare:85 | ||||
| chr6:160991643-160991789 | Common:1; Rare:47 | ||||
| chr6:162726949-162727166 | Common:4; Rare:48 | ||||
| chr6:162727724-162728075 | Common:3; Rare:107; Clinvar:1 | ||||
| chr6:163415107-163415344 | Common:6; Rare:88 |