| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:158644665-158644957 | Common:3; Rare:117 | ||||
| chr6:158649910-158650069 | Rare:35 | ||||
| chr6:158818090-158818358 | Common:5; Rare:107 | ||||
| chr6:158999734-158999930 | Common:1; Rare:86; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:159000145-159000305 | Common:1; Rare:40 | ||||
| chr6:159693148-159693597 | Common:6; Rare:135 | ||||
| chr6:159726918-159727235 | Common:1; Rare:115 | ||||
| chr6:159727325-159727682 | Common:5; Rare:144 | ||||
| chr6:159761815-159762086 | Common:4; Rare:129 | ||||
| chr6:159789452-159790004 | Common:4; Rare:192 | ||||
| chr6:159790244-159790579 | Common:8; Rare:123 | ||||
| chr6:160991614-160991902 | Common:1; Rare:98 | ||||
| chr6:162726836-162727166 | Common:4; Rare:70 | ||||
| chr6:162727670-162727978 | Rare:124; Clinvar:4 | ||||
| chr6:166342513-166342659 | Common:3; Rare:58 |