Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:189783957-189784125 | Common:3; Rare:62; Clinvar (benign):1 | ||||
chr2:189784234-189784585 | Common:4; Rare:119; Clinvar:8; Clinvar (benign):3 | ||||
chr2:190319721-190319932 | Common:4; Rare:74; Clinvar (benign):5 | ||||
chr2:190343862-190344031 | Rare:34 | ||||
chr2:190344074-190344130 | Rare:13 | ||||
chr2:190648465-190648520 | Common:2; Rare:19 | ||||
chr2:190648656-190648916 | Common:1; Rare:92 | ||||
chr2:190880536-190880893 | Common:4; Rare:117 | ||||
chr2:191014140-191014340 | Common:2; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
chr2:191245027-191245173 | Common:1; Rare:33 | ||||
chr2:191245249-191245588 | Common:2; Rare:108 | ||||
chr2:191246152-191246259 | Rare:39 | ||||
chr2:191677858-191678140 | Common:4; Rare:78 | ||||
chr2:192194886-192195058 | Rare:36 | ||||
chr2:196068820-196069059 | Common:1; Rare:70 |