Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:140107738-140107846 | Rare:32 | ||||
chr5:140303050-140303160 | Common:1; Rare:38 | ||||
chr5:140557396-140557537 | Common:1; Rare:93 | ||||
chr5:140564332-140564549 | Common:1; Rare:51 | ||||
chr5:140564556-140564855 | Rare:78 | ||||
chr5:140647590-140648073 | Common:19; Rare:188; Clinvar:4; Clinvar (benign):3 | ||||
chr5:140691300-140691708 | Common:1; Rare:149; Clinvar:12; Clinvar (benign):2 | ||||
chr5:141320725-141320962 | Common:3; Rare:84 | ||||
chr5:141636810-141637006 | Common:2; Rare:86 | ||||
chr5:141637335-141637452 | Common:1; Rare:26 | ||||
chr5:141682187-141682328 | Common:1; Rare:47 | ||||
chr5:141923701-141923890 | Common:1; Rare:51 | ||||
chr5:142012955-142013100 | Rare:46 | ||||
chr5:142324979-142325238 | Rare:86 | ||||
chr5:143404427-143404604 | Common:2; Rare:42 |