Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:107989686-107989900 | Common:5; Rare:102; Clinvar:4; Clinvar (benign):5 | ||||
chr4:108620393-108620604 | Common:6; Rare:103 | ||||
chr4:112636888-112637182 | Common:1; Rare:79 | ||||
chr4:118685349-118685413 | Common:1; Rare:21 | ||||
chr4:120066775-120066955 | Common:3; Rare:54 | ||||
chr4:121801274-121801396 | Common:2; Rare:37 | ||||
chr4:122922982-122923101 | Common:1; Rare:32 | ||||
chr4:129093519-129093731 | Rare:63 | ||||
chr4:139301231-139301546 | Common:4; Rare:89 | ||||
chr4:140523977-140524218 | Common:2; Rare:73 | ||||
chr4:142405400-142405632 | Common:1; Rare:40 | ||||
chr4:145098144-145098348 | Rare:72 | ||||
chr4:147684133-147684292 | Rare:63 | ||||
chr4:152679935-152680122 | Rare:44 | ||||
chr4:152779796-152780005 | Common:1; Rare:55 |