Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:71068537-71068678 | Rare:62 | ||||
chr2:71130220-71130673 | Common:6; Rare:128; Clinvar:1; Clinvar (benign):2 | ||||
chr2:71130679-71130698 | Common:1; Rare:7 | ||||
chr2:71453503-71453965 | Common:2; Rare:92; Clinvar (benign):2 | ||||
chr2:73071693-73071857 | Common:2; Rare:64 | ||||
chr2:73234195-73234381 | Common:2; Rare:59 | ||||
chr2:73234561-73234690 | Rare:45 | ||||
chr2:73828804-73829049 | Common:1; Rare:59 | ||||
chr2:74147866-74148111 | Common:1; Rare:67; Clinvar:2 | ||||
chr2:74178800-74179059 | Common:3; Rare:78 | ||||
chr2:74465350-74465436 | Rare:24; Clinvar:1 | ||||
chr2:74482982-74483112 | Rare:50 | ||||
chr2:74529653-74529988 | Rare:105; Clinvar:3; Clinvar (benign):1 | ||||
chr2:74958584-74958707 | Common:3; Rare:54 | ||||
chr2:74958876-74958930 | Rare:34 |