Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:137618854-137619024 | Common:1; Rare:68 | ||||
chrM:2616-3075 | |||||
chrM:3209-3219 | |||||
chrM:5385-5581 | |||||
chrM:7467-7586 | |||||
chrX:41334081-41334165 | Rare:16 | ||||
chrX:70289888-70289972 | Rare:21 | ||||
chrX:81201889-81202192 | Rare:52 | ||||
chrX:101407907-101408264 | Common:5; Rare:63; Clinvar (benign):9 | ||||
chrX:108091504-108091818 | Rare:85 | ||||
chrX:119574396-119574581 | Rare:39 | ||||
chrX:119871687-119871862 | Common:1; Rare:34 | ||||
chrX:135973751-135973879 | Rare:40 | ||||
chrX:152830718-152831002 | Common:1; Rare:49 | ||||
chrX:153794356-153794684 | Common:1; Rare:99; Clinvar (benign):2 |