| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:113627076-113627266 | Common:1; Rare:51 | ||||
| chr2:113756566-113756823 | Common:4; Rare:89 | ||||
| chr2:113889709-113890165 | Common:8; Rare:152 | ||||
| chr2:118088403-118088529 | Rare:34 | ||||
| chr2:119223753-119223840 | Rare:27 | ||||
| chr2:119366779-119367068 | Common:1; Rare:90 | ||||
| chr2:119759782-119759909 | Common:1; Rare:40 | ||||
| chr2:121530607-121530886 | Common:7; Rare:117 | ||||
| chr2:121649426-121649645 | Common:2; Rare:65 | ||||
| chr2:121736744-121737220 | Common:5; Rare:192 | ||||
| chr2:127294088-127294214 | Common:2; Rare:50; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127811139-127811259 | Rare:37 | ||||
| chr2:127885886-127885982 | Rare:24 | ||||
| chr2:128091022-128091360 | Common:8; Rare:113 | ||||
| chr2:130181546-130181760 | Common:2; Rare:99 |