Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:30231587-30231732 | Rare:36 | ||||
chr2:30447191-30447326 | Rare:41 | ||||
chr2:30807385-30807674 | Rare:63 | ||||
chr2:31233970-31234183 | Rare:55 | ||||
chr2:32010821-32011106 | Common:1; Rare:83 | ||||
chr2:32039421-32039917 | Rare:143 | ||||
chr2:32063345-32063704 | Common:1; Rare:125; Clinvar:1 | ||||
chr2:32064056-32064171 | Rare:53; Clinvar:2; Clinvar (benign):2 | ||||
chr2:32165665-32165906 | Common:1; Rare:96 | ||||
chr2:32277743-32277975 | Common:1; Rare:58 | ||||
chr2:32357105-32357241 | Common:1; Rare:55 | ||||
chr2:32627926-32628371 | Rare:132 | ||||
chr2:33599175-33599370 | Rare:78 | ||||
chr2:33599373-33599470 | Common:1; Rare:31 | ||||
chr2:36355557-36356100 | Common:4; Rare:187 |