Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:108719395-108719586 | Common:3; Rare:79; Clinvar (benign):2 | ||||
chr2:109613885-109613998 | Common:1; Rare:41 | ||||
chr2:111122443-111122747 | Common:3; Rare:126 | ||||
chr2:111884156-111884237 | Rare:22 | ||||
chr2:111898339-111898660 | Common:2; Rare:72 | ||||
chr2:112275408-112275621 | Common:1; Rare:65 | ||||
chr2:112584348-112584633 | Common:1; Rare:78 | ||||
chr2:112584772-112584917 | Rare:33 | ||||
chr2:112645688-112645944 | Common:1; Rare:92 | ||||
chr2:113627082-113627303 | Common:3; Rare:63 | ||||
chr2:113756507-113756790 | Common:4; Rare:95 | ||||
chr2:113889710-113890179 | Common:8; Rare:152 | ||||
chr2:118014037-118014166 | Common:2; Rare:90 | ||||
chr2:118088319-118088540 | Common:1; Rare:62 | ||||
chr2:119366742-119367068 | Common:1; Rare:99 |