Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:70281841-70281850 | |||||
chr2:70948564-70948875 | Common:2; Rare:74 | ||||
chr2:71421291-71421351 | Common:2; Rare:13 | ||||
chr2:71422419-71422597 | Common:1; Rare:36 | ||||
chr2:72148908-72149093 | Rare:41 | ||||
chr2:72302684-72302860 | Rare:30 | ||||
chr2:73951752-73951860 | Rare:15 | ||||
chr2:73984958-73985192 | Rare:66 | ||||
chr2:74370797-74371204 | Common:2; Rare:113; Clinvar:5; Clinvar (benign):5 | ||||
chr2:74387588-74387649 | Common:1; Rare:6 | ||||
chr2:74503954-74504211 | Common:2; Rare:54 | ||||
chr2:74960074-74960145 | Rare:19 | ||||
chr2:75239031-75239341 | Rare:75 | ||||
chr2:75239359-75239440 | Rare:14 | ||||
chr2:75664708-75664838 | Rare:42 |