| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:182867163-182867242 | Rare:19 | ||||
| chr2:183124249-183124452 | Common:4; Rare:68 | ||||
| chr2:186486037-186486364 | Common:3; Rare:97 | ||||
| chr2:188291628-188292088 | Common:6; Rare:130 | ||||
| chr2:188292597-188292855 | Common:1; Rare:58 | ||||
| chr2:189783973-189784061 | Common:2; Rare:27 | ||||
| chr2:189784281-189784537 | Common:4; Rare:92; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190319744-190319983 | Common:5; Rare:85; Clinvar (benign):5 | ||||
| chr2:191014133-191014353 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191677858-191678155 | Common:4; Rare:85 | ||||
| chr2:197434970-197435194 | Rare:75 | ||||
| chr2:197499807-197500430 | Common:1; Rare:239; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197515780-197516107 | Common:2; Rare:113 | ||||
| chr2:199911125-199911409 | Rare:91 | ||||
| chr2:200509913-200510263 | Common:2; Rare:119 |