Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:101917545-101917582 | Rare:9 | ||||
chr13:102394467-102394660 | Common:1; Rare:76 | ||||
chr13:108495117-108495148 | Rare:7 | ||||
chr13:110308524-110308678 | Common:1; Rare:28 | ||||
chr13:112106669-112106808 | Rare:28 | ||||
chr13:112942784-112942978 | Common:2; Rare:38 | ||||
chr14:22449649-22449798 | Common:1; Rare:21 | ||||
chr14:23430748-23430923 | Common:1; Rare:30; Clinvar (benign):4 | ||||
chr14:23487285-23487489 | Common:1; Rare:37 | ||||
chr14:24006942-24007140 | Common:3; Rare:51 | ||||
chr14:26873439-26873443 | |||||
chr14:32203246-32203650 | Common:13; Rare:179 | ||||
chr14:41604896-41604931 | Rare:5 | ||||
chr14:41605274-41605375 | Common:3; Rare:16 | ||||
chr14:41610006-41610134 | Rare:36 |