Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:237487187-237487287 | Common:1; Rare:28 | ||||
chr2:238426892-238427067 | Common:1; Rare:65 | ||||
chr2:240025289-240025429 | Common:1; Rare:57; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr2:240560766-240560906 | Common:2; Rare:64 | ||||
chr2:241272794-241272971 | Rare:69 | ||||
chr2:241315119-241315281 | Common:1; Rare:60 | ||||
chr2:241315632-241315994 | Common:5; Rare:139 | ||||
chr20:380976-381109 | Common:2; Rare:34 | ||||
chr20:408265-408375 | Common:1; Rare:26 | ||||
chr20:1118457-1118660 | Common:3; Rare:63 | ||||
chr20:1325260-1325426 | Rare:40 | ||||
chr20:1392960-1393281 | Common:2; Rare:127 | ||||
chr20:2652438-2652663 | Common:8; Rare:79 | ||||
chr20:2840672-2840756 | Common:1; Rare:35 | ||||
chr20:3209258-3209542 | Common:3; Rare:76 |