Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:84690365-84690712 | Rare:113 | ||||
chr1:85048416-85048617 | Common:2; Rare:45 | ||||
chr1:85048663-85048697 | Rare:6 | ||||
chr1:85276296-85276641 | Common:5; Rare:119; Clinvar (benign):3 | ||||
chr1:85580717-85581055 | Common:2; Rare:104 | ||||
chr1:85707815-85708281 | Common:3; Rare:134 | ||||
chr1:85708288-85708495 | Common:2; Rare:73 | ||||
chr1:86356163-86356207 | Rare:3 | ||||
chr1:86356355-86356563 | Common:4; Rare:65 | ||||
chr1:86424042-86424431 | Rare:89 | ||||
chr1:86704433-86704645 | Rare:88 | ||||
chr1:86704707-86704966 | Common:3; Rare:93 | ||||
chr1:86914293-86914778 | Common:3; Rare:146 | ||||
chr1:86915076-86915124 | Rare:16 | ||||
chr1:87328822-87329040 | Common:3; Rare:74 |