Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:629945-630208 | Common:7; Rare:47 | ||||
chr1:630624-630749 | Common:3; Rare:12 | ||||
chr1:633830-634027 | Common:3; Rare:80 | ||||
chr1:827500-827721 | Common:2; Rare:86 | ||||
chr1:16644657-16644768 | Common:1; Rare:2 | ||||
chr1:22025037-22025076 | Rare:4 | ||||
chr1:22025428-22025520 | Common:5; Rare:30 | ||||
chr1:23310991-23311287 | Rare:89 | ||||
chr1:27842932-27843212 | Rare:49 | ||||
chr1:35192229-35192295 | Common:1; Rare:29 | ||||
chr1:37809434-37809636 | Rare:28 | ||||
chr1:42752220-42752351 | Common:2; Rare:45; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:46302019-46302164 | Common:1; Rare:41 | ||||
chr1:53115861-53116109 | Common:5; Rare:54 | ||||
chr1:67831931-67832249 | Common:1; Rare:71 |