| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46616984-46617276 | Common:7; Rare:127 | ||||
| chr2:46915723-46915869 | Common:1; Rare:37; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916007-46916167 | Common:2; Rare:54 | ||||
| chr2:46941716-46941874 | Common:3; Rare:50 | ||||
| chr2:47176427-47176569 | Rare:102; Clinvar (benign):5 | ||||
| chr2:48440631-48440801 | Common:5; Rare:70 | ||||
| chr2:53767559-53767839 | Common:4; Rare:96 | ||||
| chr2:53786842-53787170 | Common:1; Rare:123 | ||||
| chr2:53970780-53971152 | Common:11; Rare:135 | ||||
| chr2:54115502-54115682 | Rare:62 | ||||
| chr2:55050302-55050376 | Rare:33 | ||||
| chr2:55050428-55050737 | Common:4; Rare:93 | ||||
| chr2:55232284-55232872 | Common:4; Rare:186 | ||||
| chr2:58241311-58241420 | Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:61017420-61017753 | Common:1; Rare:100; Clinvar:2 |