| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:158819325-158819450 | Common:2; Rare:47 | ||||
| chr6:158999746-158999981 | Common:1; Rare:104; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:159693233-159693609 | Common:5; Rare:111 | ||||
| chr6:159726847-159727175 | Common:1; Rare:142 | ||||
| chr6:159727315-159727637 | Common:5; Rare:136 | ||||
| chr6:159761775-159762103 | Common:5; Rare:154 | ||||
| chr6:159762304-159762593 | Common:2; Rare:80 | ||||
| chr6:159780441-159780703 | Common:1; Rare:71 | ||||
| chr6:159789538-159790004 | Common:4; Rare:155 | ||||
| chr6:159790244-159790631 | Common:11; Rare:149 | ||||
| chr6:159968892-159969082 | Common:1; Rare:78 | ||||
| chr6:161273747-161273844 | Common:1; Rare:26 | ||||
| chr6:161273943-161274181 | Rare:43 | ||||
| chr6:162727706-162727974 | Rare:96; Clinvar:3 | ||||
| chr6:166342496-166342681 | Common:3; Rare:75 |