Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:227325199-227325323 | Common:3; Rare:42 | ||||
chr2:229921924-229922282 | Common:2; Rare:143 | ||||
chr2:229922404-229922513 | Rare:33 | ||||
chr2:230219931-230220017 | Rare:12 | ||||
chr2:230468782-230469089 | Common:8; Rare:52 | ||||
chr2:231460256-231460865 | Common:4; Rare:279 | ||||
chr2:231464405-231464763 | Common:3; Rare:120 | ||||
chr2:231781236-231781436 | Rare:59 | ||||
chr2:232550553-232550723 | Rare:65 | ||||
chr2:237085758-237085976 | Common:2; Rare:81 | ||||
chr2:237413954-237414298 | Common:2; Rare:68; Clinvar (benign):3 | ||||
chr2:237487044-237487276 | Common:4; Rare:51 | ||||
chr2:237627520-237627661 | Common:2; Rare:49 | ||||
chr2:238426905-238427064 | Common:1; Rare:54 | ||||
chr2:238847849-238848108 | Common:1; Rare:55 |