| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:113627069-113627272 | Common:1; Rare:60 | ||||
| chr2:113756601-113756804 | Common:3; Rare:81 | ||||
| chr2:113889759-113890165 | Common:8; Rare:131 | ||||
| chr2:118014041-118014214 | Common:2; Rare:98 | ||||
| chr2:118088171-118088540 | Common:2; Rare:93 | ||||
| chr2:119366770-119367038 | Common:1; Rare:80 | ||||
| chr2:119678972-119679212 | Common:5; Rare:64 | ||||
| chr2:120252618-120252967 | Common:3; Rare:115 | ||||
| chr2:121530618-121530887 | Common:5; Rare:115 | ||||
| chr2:121649418-121649674 | Common:2; Rare:73 | ||||
| chr2:121736828-121737255 | Common:5; Rare:163 | ||||
| chr2:121755402-121755782 | Common:6; Rare:127 | ||||
| chr2:127294077-127294246 | Common:2; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387958-127388198 | Common:3; Rare:102 | ||||
| chr2:127811118-127811258 | Rare:46 |