Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156020071-156020303 | Rare:60 | ||||
chr1:156020823-156021060 | Rare:72 | ||||
chr1:156053176-156053310 | Common:1; Rare:21 | ||||
chr1:156053751-156053988 | Rare:61 | ||||
chr1:156054002-156054264 | Common:1; Rare:61 | ||||
chr1:156054281-156054470 | Rare:28 | ||||
chr1:156054530-156054885 | Common:4; Rare:96 | ||||
chr1:156054957-156055090 | Common:1; Rare:32 | ||||
chr1:156055244-156055297 | Rare:14 | ||||
chr1:156061059-156061181 | Rare:28 | ||||
chr1:156082429-156082713 | Rare:64 | ||||
chr1:156082881-156082996 | Rare:40 | ||||
chr1:156106228-156106616 | Common:2; Rare:68 | ||||
chr1:156114154-156114588 | Rare:70 | ||||
chr1:156114592-156114910 | Common:1; Rare:76; Clinvar:4; Clinvar (benign):4 |