| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:112087410-112087684 | Rare:91 | ||||
| chr6:113857247-113857407 | Common:1; Rare:37 | ||||
| chr6:113970592-113970817 | Rare:70 | ||||
| chr6:113971074-113971449 | Common:3; Rare:130 | ||||
| chr6:116100720-116100903 | Common:1; Rare:67 | ||||
| chr6:116254053-116254222 | Common:4; Rare:45 | ||||
| chr6:116279423-116279507 | Common:1; Rare:33 | ||||
| chr6:116279535-116279606 | Rare:19 | ||||
| chr6:116279856-116280114 | Common:2; Rare:84 | ||||
| chr6:116370738-116371045 | Rare:77 | ||||
| chr6:117265397-117265559 | Common:1; Rare:35 | ||||
| chr6:117602176-117602241 | Rare:27 | ||||
| chr6:118548201-118548390 | Common:2; Rare:38; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:118894084-118894309 | Common:1; Rare:54 | ||||
| chr6:119349732-119349936 | Common:3; Rare:73 |