Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:235417187-235417287 | Rare:10 | ||||
chr1:235489996-235490188 | Rare:35 | ||||
chr1:240093026-240093276 | Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
chr1:240212723-240212795 | Rare:20 | ||||
chr1:240253501-240253665 | Common:1; Rare:36 | ||||
chr1:240369983-240370008 | Rare:7 | ||||
chr1:243797199-243797354 | Rare:28 | ||||
chr1:243839902-243840211 | Common:1; Rare:56 | ||||
chr1:244409538-244409811 | Common:1; Rare:59 | ||||
chr1:244424033-244424329 | Common:2; Rare:61 | ||||
chr1:244427311-244427432 | Rare:23 | ||||
chr1:244451169-244451277 | Common:2; Rare:35 | ||||
chr1:245088977-245089118 | Common:1; Rare:21 | ||||
chr1:246225396-246225444 | Rare:4 | ||||
chr1:246251068-246251160 | Common:1; Rare:10 |