Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:218285178-218285449 | Common:4; Rare:111 | ||||
chr1:218345760-218346090 | Common:5; Rare:102; Clinvar:9; Clinvar (benign):4 | ||||
chr1:218346145-218346318 | Rare:27 | ||||
chr1:219173746-219173900 | Common:1; Rare:79 | ||||
chr1:219174765-219174993 | Rare:37 | ||||
chr1:220272345-220272552 | Rare:59; Clinvar:5 | ||||
chr1:220528566-220528756 | Rare:61 | ||||
chr1:220690192-220690411 | Rare:87 | ||||
chr1:220748563-220748774 | Common:2; Rare:72 | ||||
chr1:220786734-220787063 | Common:4; Rare:76 | ||||
chr1:220879199-220879332 | Common:1; Rare:35 | ||||
chr1:221742065-221742288 | Rare:59 | ||||
chr1:222589771-222589990 | Common:2; Rare:60 | ||||
chr1:222617849-222618131 | Common:3; Rare:73 | ||||
chr1:222644109-222644412 | Common:2; Rare:89 |