Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:77889863-77890110 | Rare:29 | ||||
chr1:77925136-77925225 | Common:1; Rare:25; Clinvar (benign):1 | ||||
chr1:77939127-77939254 | Common:1; Rare:30 | ||||
chr1:77944079-77944453 | Common:1; Rare:57 | ||||
chr1:77944687-77944962 | Rare:53 | ||||
chr1:77951853-77951910 | Rare:8 | ||||
chr1:77952273-77952358 | Rare:15 | ||||
chr1:77964873-77965229 | Common:3; Rare:94 | ||||
chr1:77966711-77966957 | Common:2; Rare:55 | ||||
chr1:77969907-77970093 | Common:1; Rare:46 | ||||
chr1:77978353-77978401 | Rare:18 | ||||
chr1:78005831-78005916 | Rare:19 | ||||
chr1:78006254-78006280 | Rare:6 | ||||
chr1:78007625-78007754 | Common:1; Rare:21 | ||||
chr1:78015469-78015497 | Rare:1 |