| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:46652789-46653008 | Rare:55 | ||||
| chr6:73394597-73394894 | Common:4; Rare:95 | ||||
| chr6:82364075-82364255 | Common:2; Rare:43 | ||||
| chr6:83193192-83193416 | Common:3; Rare:76 | ||||
| chr6:87589965-87590171 | Common:3; Rare:89; Clinvar (benign):3 | ||||
| chr6:106629469-106629588 | Common:1; Rare:23 | ||||
| chr6:107958061-107958383 | Common:2; Rare:97; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:109691151-109691296 | Common:1; Rare:34; Clinvar (benign):1 | ||||
| chr6:111483142-111483617 | Common:1; Rare:168 | ||||
| chr6:112087463-112087684 | Rare:63 | ||||
| chr6:113857304-113857442 | Common:1; Rare:29 | ||||
| chr6:116370602-116370910 | Common:1; Rare:62 | ||||
| chr6:119349732-119349900 | Common:2; Rare:57 | ||||
| chr6:121435527-121435806 | Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:127343334-127343411 | Rare:12 |