Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:20651054-20651287 | Rare:71 | ||||
chr2:20823055-20823159 | Rare:42 | ||||
chr2:23927073-23927325 | Common:3; Rare:88 | ||||
chr2:23940306-23940538 | Common:4; Rare:79 | ||||
chr2:24076205-24076587 | Rare:104 | ||||
chr2:24123282-24123522 | Common:1; Rare:65 | ||||
chr2:24793025-24793161 | Rare:58 | ||||
chr2:24971907-24972138 | Common:1; Rare:75 | ||||
chr2:25878453-25878648 | Common:1; Rare:61 | ||||
chr2:26033753-26034167 | Common:4; Rare:157 | ||||
chr2:26195219-26195395 | Rare:49; Clinvar (benign):1 | ||||
chr2:26244585-26244974 | Common:2; Rare:142; Clinvar:5; Clinvar (benign):8 | ||||
chr2:26345798-26346156 | Common:1; Rare:107 | ||||
chr2:26764178-26764325 | Common:1; Rare:58 | ||||
chr2:27032862-27033004 | Rare:55 |