Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40394945-40394989 | Common:1; Rare:7 | ||||
chr1:41168041-41168108 | Rare:11 | ||||
chr1:42980457-42980474 | Rare:3 | ||||
chr1:43439539-43439668 | Common:1; Rare:25; Clinvar:1; Clinvar (benign):1 | ||||
chr1:43523220-43523491 | Rare:56 | ||||
chr1:43594156-43594408 | Common:6; Rare:29 | ||||
chr1:43597045-43597270 | Common:3; Rare:68 | ||||
chr1:44030016-44030134 | Rare:46 | ||||
chr1:44030165-44030457 | Rare:100 | ||||
chr1:44238188-44238498 | Common:2; Rare:92 | ||||
chr1:45303557-45303855 | Common:1; Rare:81 | ||||
chr1:45973252-45973731 | Common:2; Rare:103 | ||||
chr1:46008308-46008461 | Rare:46 | ||||
chr1:46010038-46010472 | Common:1; Rare:66 | ||||
chr1:46026401-46026459 | Rare:8 |