Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40097555-40097955 | Common:1; Rare:94 | ||||
chr1:40161156-40161481 | Common:1; Rare:108 | ||||
chr1:40257898-40258282 | Common:4; Rare:105; Clinvar:8; Clinvar (benign):1 | ||||
chr1:40315357-40315575 | Common:4; Rare:49 | ||||
chr1:40373493-40373790 | Common:1; Rare:72 | ||||
chr1:40374450-40374830 | Common:13; Rare:76 | ||||
chr1:40449883-40450387 | Common:8; Rare:166 | ||||
chr1:40450628-40450936 | Common:2; Rare:63 | ||||
chr1:40477020-40477410 | Common:4; Rare:102 | ||||
chr1:40508646-40508789 | Common:3; Rare:38 | ||||
chr1:40531473-40531743 | Common:1; Rare:74 | ||||
chr1:40531808-40532208 | Rare:80 | ||||
chr1:40665647-40665802 | Common:1; Rare:45 | ||||
chr1:40691410-40691890 | Common:3; Rare:200 | ||||
chr1:40692022-40692263 | Common:2; Rare:80 |