Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:128083040-128083159 | Common:2; Rare:34 | ||||
chr5:132829286-132829335 | Rare:7 | ||||
chr5:132841360-132841421 | Rare:14 | ||||
chr5:134927172-134927353 | Common:1; Rare:31 | ||||
chr5:138493183-138493371 | Common:1; Rare:36 | ||||
chr5:139747952-139748222 | Common:2; Rare:58 | ||||
chr5:140596369-140596731 | Common:2; Rare:61 | ||||
chr5:141413760-141413927 | Common:1; Rare:45 | ||||
chr5:141528451-141528940 | Rare:126; Clinvar:5; Clinvar (benign):6 | ||||
chr5:148826351-148826632 | Common:4; Rare:67 | ||||
chr5:149135515-149135814 | Rare:55 | ||||
chr5:149149983-149150209 | Common:2; Rare:34 | ||||
chr5:149161166-149161303 | Rare:18 | ||||
chr5:150715600-150715862 | Common:2; Rare:60 | ||||
chr5:150778680-150778863 | Rare:71 |