Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:71069204-71069320 | Rare:30 | ||||
chr1:71080988-71081376 | Rare:101 | ||||
chr1:72282017-72282248 | Common:1; Rare:53 | ||||
chr1:72282490-72282554 | Rare:28 | ||||
chr1:72282845-72282973 | Common:3; Rare:51 | ||||
chr1:74198105-74198368 | Common:3; Rare:138 | ||||
chr1:74732815-74733346 | Common:6; Rare:166 | ||||
chr1:74733369-74733488 | Rare:47 | ||||
chr1:75786904-75787071 | Common:2; Rare:46 | ||||
chr1:77219400-77219536 | Rare:59 | ||||
chr1:77281933-77282351 | Common:3; Rare:111 | ||||
chr1:77370968-77371348 | Common:1; Rare:58 | ||||
chr1:77888164-77888394 | Common:1; Rare:50 | ||||
chr1:77888402-77888774 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
chr1:77926516-77926773 | Common:1; Rare:72; Clinvar:8; Clinvar (benign):6 |