Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:94820264-94820369 | Common:2; Rare:28 | ||||
chr1:95072857-95073018 | Common:1; Rare:66; Clinvar (benign):2 | ||||
chr1:95233955-95234233 | Common:5; Rare:83 | ||||
chr1:96721580-96721844 | Common:2; Rare:124 | ||||
chr1:98661578-98661869 | Common:2; Rare:102 | ||||
chr1:100037984-100038143 | Common:1; Rare:65 | ||||
chr1:100132902-100133202 | Common:2; Rare:107 | ||||
chr1:100266114-100266332 | Common:2; Rare:78 | ||||
chr1:100894778-100895014 | Common:1; Rare:50 | ||||
chr1:101025763-101025910 | Common:1; Rare:44 | ||||
chr1:103525500-103525727 | Rare:57 | ||||
chr1:108200219-108200429 | Common:8; Rare:58 | ||||
chr1:108661045-108661131 | Rare:29 | ||||
chr1:108692197-108692368 | Common:1; Rare:69 | ||||
chr1:108963418-108963611 | Rare:68 |