Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:2223173-2223725 | Rare:202 | ||||
chr16:2224067-2224233 | Rare:33 | ||||
chr16:2251530-2251779 | Rare:91 | ||||
chr16:2267764-2267953 | Common:3; Rare:65 | ||||
chr16:2268014-2268243 | Common:1; Rare:100 | ||||
chr16:2268322-2268595 | Common:4; Rare:94 | ||||
chr16:2340652-2340942 | Common:2; Rare:107; Clinvar:3; Clinvar (benign):2 | ||||
chr16:2428940-2429002 | Rare:12 | ||||
chr16:2429027-2429549 | Common:4; Rare:165 | ||||
chr16:2459908-2460167 | Common:2; Rare:85 | ||||
chr16:2460274-2460416 | Common:1; Rare:53 | ||||
chr16:2474935-2475164 | Rare:71; Clinvar (benign):2 | ||||
chr16:2475545-2475580 | Rare:10 | ||||
chr16:2513535-2514078 | Rare:214 | ||||
chr16:2514186-2514269 | Rare:32 |