Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228416742-228417059 | Rare:55 | ||||
chr1:228457866-228458113 | Common:1; Rare:78 | ||||
chr1:228487081-228487590 | Common:4; Rare:148 | ||||
chr1:229270997-229271351 | Rare:112 | ||||
chr1:229508284-229508498 | Common:1; Rare:86 | ||||
chr1:229518841-229519088 | Rare:43 | ||||
chr1:229625902-229626284 | Rare:128 | ||||
chr1:230642258-230642597 | Common:1; Rare:119 | ||||
chr1:230868181-230868577 | Rare:134 | ||||
chr1:230868987-230869136 | Common:2; Rare:29 | ||||
chr1:230869543-230869727 | Rare:36 | ||||
chr1:230978834-230979098 | Common:1; Rare:92 | ||||
chr1:231040203-231040340 | Common:1; Rare:45 | ||||
chr1:231241087-231241382 | Common:2; Rare:142; Clinvar:5; Clinvar (benign):2 | ||||
chr1:231337795-231338497 | Common:4; Rare:227 |