| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:113971127-113971495 | Common:3; Rare:116 | ||||
| chr6:116100695-116100909 | Common:1; Rare:80 | ||||
| chr6:116254044-116254183 | Common:3; Rare:35 | ||||
| chr6:116279413-116279503 | Common:1; Rare:38 | ||||
| chr6:116279505-116279617 | Common:1; Rare:37 | ||||
| chr6:116279835-116280086 | Common:1; Rare:88 | ||||
| chr6:117602131-117602191 | Rare:13 | ||||
| chr6:117602471-117602670 | Common:3; Rare:56 | ||||
| chr6:117675310-117675501 | Common:3; Rare:52 | ||||
| chr6:118548084-118548332 | Common:1; Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:118893926-118894292 | Common:2; Rare:108 | ||||
| chr6:118934987-118935071 | Common:4; Rare:28 | ||||
| chr6:119349732-119349926 | Common:2; Rare:67 | ||||
| chr6:121334437-121334552 | Common:2; Rare:54 | ||||
| chr6:122399351-122399708 | Common:6; Rare:135 |