Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145995118-145995479 | Rare:143 | ||||
chr1:145995998-145996607 | Common:1; Rare:244 | ||||
chr1:145996666-145996808 | Rare:45 | ||||
chr1:147172295-147172823 | Common:1; Rare:141 | ||||
chr1:147225308-147225669 | Common:3; Rare:67 | ||||
chr1:147541205-147541561 | Common:2; Rare:56 | ||||
chr1:147670024-147670321 | Common:1; Rare:68 | ||||
chr1:148952021-148952141 | Common:3; Rare:32 | ||||
chr1:148952235-148952635 | Common:5; Rare:106 | ||||
chr1:149812150-149812560 | Common:2; Rare:177 | ||||
chr1:149842748-149842939 | Rare:3 | ||||
chr1:149850856-149851062 | Rare:1 | ||||
chr1:149886600-149887245 | Common:3; Rare:240 | ||||
chr1:149887894-149888215 | Rare:99 | ||||
chr1:149927756-149927901 | Common:1; Rare:60; Clinvar (benign):5 |