| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178451090-178451369 | Common:6; Rare:83; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478527-178478671 | Common:1; Rare:46 | ||||
| chr2:179264502-179264857 | Common:4; Rare:131 | ||||
| chr2:180980279-180980545 | Common:1; Rare:86 | ||||
| chr2:182866548-182866828 | Common:1; Rare:63 | ||||
| chr2:186485987-186486373 | Common:3; Rare:113 | ||||
| chr2:187448142-187448396 | Rare:39 | ||||
| chr2:188291595-188292049 | Common:6; Rare:128 | ||||
| chr2:188292969-188293083 | Rare:15 | ||||
| chr2:189441094-189441511 | Common:2; Rare:127 | ||||
| chr2:189580742-189580891 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:189783965-189784085 | Common:3; Rare:42; Clinvar (benign):1 | ||||
| chr2:189784281-189784537 | Common:4; Rare:92; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190180729-190181105 | Rare:109 | ||||
| chr2:190319729-190319954 | Common:5; Rare:82; Clinvar (benign):5 |