Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160190971-160191027 | Common:1; Rare:20 | ||||
chr1:160261562-160261761 | Common:1; Rare:40 | ||||
chr1:160262111-160262241 | Rare:34 | ||||
chr1:160262401-160262636 | Common:1; Rare:72 | ||||
chr1:160284197-160284390 | Common:1; Rare:31 | ||||
chr1:160285086-160285484 | Common:5; Rare:102; Clinvar:2; Clinvar (benign):4 | ||||
chr1:160343163-160343478 | Rare:130 | ||||
chr1:160400364-160400615 | Common:1; Rare:62 | ||||
chr1:160400742-160400806 | Rare:9 | ||||
chr1:160647012-160647096 | Rare:15 | ||||
chr1:160711771-160711935 | Common:2; Rare:39 | ||||
chr1:161021012-161021260 | Common:5; Rare:80 | ||||
chr1:161045874-161046057 | Common:1; Rare:48 | ||||
chr1:161069634-161069751 | Rare:24 | ||||
chr1:161089526-161089740 | Rare:47 |