Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:159615216-159615314 | Common:2; Rare:21 | ||||
chr2:159615475-159615659 | Common:2; Rare:61 | ||||
chr2:159616419-159616512 | Common:1; Rare:23 | ||||
chr2:159712346-159712606 | Common:2; Rare:96 | ||||
chr2:161308390-161308590 | Common:2; Rare:46 | ||||
chr2:162073986-162074028 | Rare:15 | ||||
chr2:162318650-162318763 | Rare:20 | ||||
chr2:164955423-164955658 | Rare:53 | ||||
chr2:169479377-169479556 | Common:3; Rare:71; Clinvar (benign):1 | ||||
chr2:169584709-169584852 | Rare:42 | ||||
chr2:169694383-169694579 | Common:5; Rare:57 | ||||
chr2:169798648-169798979 | Rare:81 | ||||
chr2:171433941-171434342 | Common:3; Rare:107 | ||||
chr2:171434744-171434823 | Rare:18 | ||||
chr2:171999837-171999964 | Common:1; Rare:55 |