Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:99180967-99181231 | Common:2; Rare:79 | ||||
chr2:100562798-100563070 | Common:3; Rare:95 | ||||
chr2:101002167-101002318 | Rare:58 | ||||
chr2:101002530-101002737 | Rare:50 | ||||
chr2:101109954-101110090 | Common:2; Rare:27 | ||||
chr2:101252658-101252907 | Common:5; Rare:82 | ||||
chr2:102736851-102736922 | Common:1; Rare:26 | ||||
chr2:105037833-105038118 | Common:3; Rare:101 | ||||
chr2:105337459-105337616 | Common:1; Rare:75 | ||||
chr2:106194243-106194568 | Common:6; Rare:138 | ||||
chr2:108449110-108449277 | Rare:68 | ||||
chr2:108534194-108534551 | Common:8; Rare:140 | ||||
chr2:108719414-108719678 | Common:2; Rare:111; Clinvar (benign):2 | ||||
chr2:109613871-109614009 | Common:2; Rare:46 | ||||
chr2:111122484-111122788 | Common:2; Rare:119 |