Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:52365189-52365461 | Common:1; Rare:52 | ||||
chr1:52651396-52651445 | Rare:14 | ||||
chr1:52772663-52772773 | Rare:29 | ||||
chr1:52801917-52802140 | Rare:44 | ||||
chr1:52880094-52880257 | Common:3; Rare:19 | ||||
chr1:52908659-52908759 | Rare:20 | ||||
chr1:52908963-52909093 | Common:2; Rare:24 | ||||
chr1:52920334-52920640 | Rare:53 | ||||
chr1:52947084-52947233 | Common:2; Rare:9 | ||||
chr1:53027715-53028068 | Common:6; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
chr1:53047179-53047239 | Rare:8 | ||||
chr1:53235619-53235942 | Common:1; Rare:53 | ||||
chr1:53701819-53701921 | Rare:26 | ||||
chr1:53947045-53947293 | Rare:41 | ||||
chr1:53975291-53975392 | Rare:18 |