| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109691151-109691319 | Common:3; Rare:41; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110958680-110958764 | Common:1; Rare:32 | ||||
| chr6:110981908-110982114 | Common:3; Rare:100 | ||||
| chr6:112087452-112087684 | Rare:71 | ||||
| chr6:113971106-113971494 | Common:3; Rare:122 | ||||
| chr6:116100695-116100910 | Common:1; Rare:81 | ||||
| chr6:116254068-116254232 | Common:4; Rare:42 | ||||
| chr6:116279850-116280084 | Common:1; Rare:79 | ||||
| chr6:116370744-116370976 | Rare:57 | ||||
| chr6:116571175-116571593 | Common:3; Rare:121 | ||||
| chr6:118574037-118574469 | Common:2; Rare:95 | ||||
| chr6:118893926-118894225 | Common:1; Rare:88 | ||||
| chr6:119349732-119349900 | Common:2; Rare:57 | ||||
| chr6:121334462-121334543 | Common:2; Rare:32 | ||||
| chr6:122399351-122399708 | Common:6; Rare:135 |