Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:133149103-133149294 | Common:2; Rare:55 | ||||
chr4:138242240-138242552 | Common:1; Rare:67 | ||||
chr4:139301301-139301574 | Common:3; Rare:86 | ||||
chr4:139453686-139454185 | Common:5; Rare:133; Clinvar:10; Clinvar (benign):4 | ||||
chr4:139556160-139556522 | Rare:69 | ||||
chr4:140373374-140373700 | Common:2; Rare:130 | ||||
chr4:141636282-141636735 | Common:3; Rare:102 | ||||
chr4:142405400-142405543 | Rare:24 | ||||
chr4:143184646-143184914 | Common:9; Rare:107 | ||||
chr4:143513614-143513765 | Rare:46 | ||||
chr4:145098129-145098379 | Rare:81 | ||||
chr4:145619161-145619406 | Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
chr4:146521864-146521976 | Rare:23 | ||||
chr4:147617225-147617479 | Common:1; Rare:58 | ||||
chr4:147684109-147684309 | Common:1; Rare:85 |