Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:113761047-113761232 | Rare:54 | ||||
chr4:119135780-119135982 | Common:1; Rare:29; Clinvar (benign):3 | ||||
chr4:119212554-119212865 | Common:4; Rare:72 | ||||
chr4:119213124-119213330 | Rare:30 | ||||
chr4:119628802-119628944 | Common:3; Rare:58 | ||||
chr4:120066825-120066973 | Common:4; Rare:37 | ||||
chr4:120067190-120067211 | Rare:3 | ||||
chr4:122732432-122732768 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
chr4:122922945-122923139 | Common:2; Rare:62 | ||||
chr4:128060979-128061325 | Common:1; Rare:125 | ||||
chr4:128811162-128811332 | Rare:36 | ||||
chr4:129093524-129093736 | Rare:63 | ||||
chr4:139177183-139177447 | Rare:78 | ||||
chr4:139301183-139301583 | Common:6; Rare:114 | ||||
chr4:139386080-139386193 | Rare:28 |