Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:202912127-202912554 | Common:4; Rare:127 | ||||
chr2:203014643-203014931 | Common:1; Rare:92 | ||||
chr2:203238719-203239054 | Common:2; Rare:110 | ||||
chr2:203239213-203239344 | Rare:42 | ||||
chr2:203328190-203328453 | Common:2; Rare:96 | ||||
chr2:203535250-203535569 | Common:3; Rare:136 | ||||
chr2:205682356-205682747 | Rare:83 | ||||
chr2:205682913-205683170 | Common:1; Rare:34 | ||||
chr2:206085772-206085971 | Common:1; Rare:57 | ||||
chr2:206086098-206086204 | Rare:12 | ||||
chr2:206086275-206086406 | Rare:22 | ||||
chr2:206159347-206160036 | Common:4; Rare:204; Clinvar (benign):1 | ||||
chr2:206274916-206275041 | Rare:47 | ||||
chr2:206765273-206765668 | Common:3; Rare:110; Clinvar:4; Clinvar (benign):5 | ||||
chr2:207165758-207166088 | Rare:64 |