Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:202238498-202238670 | Rare:58 | ||||
chr2:202912147-202912281 | Common:1; Rare:49 | ||||
chr2:203238961-203239026 | Rare:28 | ||||
chr2:206159384-206159681 | Common:2; Rare:99 | ||||
chr2:206765311-206765637 | Common:3; Rare:79; Clinvar:4; Clinvar (benign):3 | ||||
chr2:208255069-208255232 | Common:2; Rare:45 | ||||
chr2:216498689-216498894 | Common:7; Rare:85 | ||||
chr2:218217058-218217206 | Common:1; Rare:53 | ||||
chr2:218270104-218270343 | Common:5; Rare:71 | ||||
chr2:218659600-218659737 | Rare:33 | ||||
chr2:218671968-218672037 | Rare:27 | ||||
chr2:219176926-219177087 | Common:4; Rare:49 | ||||
chr2:227325168-227325323 | Common:3; Rare:60 | ||||
chr2:231464409-231464793 | Common:3; Rare:128 | ||||
chr2:232550555-232550716 | Rare:59 |