Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45568678-45568960 | Common:1; Rare:63 | ||||
chr1:45583813-45584191 | Common:2; Rare:131 | ||||
chr1:45686411-45686490 | Rare:32 | ||||
chr1:45686492-45686668 | Rare:58 | ||||
chr1:45686988-45687351 | Common:2; Rare:91 | ||||
chr1:45688037-45688269 | Common:1; Rare:61 | ||||
chr1:46132829-46133239 | Common:3; Rare:111 | ||||
chr1:46183511-46183596 | Rare:10 | ||||
chr1:46184496-46184889 | Common:1; Rare:122 | ||||
chr1:46185170-46185938 | Common:1; Rare:180 | ||||
chr1:46192155-46192402 | Rare:81; Clinvar:8; Clinvar (pathogenic):5 | ||||
chr1:46198321-46198472 | Rare:62; Clinvar:1; Clinvar (benign):2 | ||||
chr1:46203018-46203375 | Rare:58 | ||||
chr1:46300918-46301032 | Rare:17 | ||||
chr1:46303122-46303744 | Common:3; Rare:183 |