Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:41021038-41021842 | Common:9; Rare:195 | ||||
chr1:41241357-41241894 | Common:2; Rare:173 | ||||
chr1:41241861-41242119 | Common:6; Rare:142 | ||||
chr1:41242090-41242427 | Rare:311 | ||||
chr1:41242470-41242970 | Common:7; Rare:234 | ||||
chr1:41361440-41362283 | Common:9; Rare:374 | ||||
chr1:42035474-42036228 | Common:10; Rare:420 | ||||
chr1:42334225-42334625 | Rare:135 | ||||
chr1:42334984-42336033 | Common:55; Rare:1253 | ||||
chr1:42456120-42456625 | Common:7; Rare:611 | ||||
chr1:42456640-42456800 | Rare:54 | ||||
chr1:42456820-42457240 | Common:1; Rare:189; Clinvar (pathogenic):2 | ||||
chr1:42658040-42658540 | Common:16; Rare:557 | ||||
chr1:42658550-42658820 | Rare:174 | ||||
chr1:42658772-42659172 | Common:3; Rare:210 |