Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:35094030-35094332 | Rare:67 | ||||
chr1:35186942-35187271 | Common:1; Rare:116 | ||||
chr1:35438463-35438500 | Rare:6 | ||||
chr1:36139721-36140077 | Common:3; Rare:72; Clinvar (pathogenic):1 | ||||
chr1:37575021-37575144 | Rare:20 | ||||
chr1:37809434-37809536 | Rare:15 | ||||
chr1:39115952-39116060 | Rare:17 | ||||
chr1:40267735-40267804 | Common:1; Rare:20; Clinvar:1 | ||||
chr1:40687064-40687157 | Common:1; Rare:19 | ||||
chr1:41168153-41168198 | Rare:3 | ||||
chr1:41432961-41433276 | Common:1; Rare:61 | ||||
chr1:42226331-42226474 | Common:2; Rare:28 | ||||
chr1:42500413-42500678 | Common:3; Rare:57 | ||||
chr1:42693867-42694033 | Rare:32 | ||||
chr1:42752220-42752286 | Common:2; Rare:21; Clinvar (benign):1; Clinvar (pathogenic):1 |