Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156367380-156367493 | Rare:29 | ||||
chr1:156369122-156369221 | Common:2; Rare:27 | ||||
chr1:156591475-156591986 | Common:7; Rare:183; Clinvar (pathogenic):1 | ||||
chr1:156593110-156593550 | Common:3; Rare:103 | ||||
chr1:156601413-156601504 | Common:1; Rare:37 | ||||
chr1:156725545-156725992 | Common:2; Rare:89 | ||||
chr1:156726066-156726209 | Rare:29 | ||||
chr1:156728352-156728551 | Common:1; Rare:51 | ||||
chr1:156728553-156728971 | Rare:119 | ||||
chr1:156729079-156729227 | Rare:57 | ||||
chr1:156741037-156741439 | Common:1; Rare:110 | ||||
chr1:156743743-156744023 | Common:2; Rare:71 | ||||
chr1:156747098-156747334 | Common:3; Rare:32 | ||||
chr1:156752253-156752507 | Rare:58 | ||||
chr1:156766879-156767217 | Rare:57 |