Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:138465792-138465995 | Rare:96 | ||||
chr5:138543095-138543585 | Common:2; Rare:159 | ||||
chr5:138543673-138543783 | Rare:24 | ||||
chr5:138575295-138575963 | Common:2; Rare:234 | ||||
chr5:138753290-138753481 | Common:2; Rare:62 | ||||
chr5:138875265-138875496 | Rare:46; Clinvar (benign):1 | ||||
chr5:139198288-139198525 | Rare:79; Clinvar (benign):1 | ||||
chr5:139293528-139294035 | Rare:160 | ||||
chr5:139294403-139294748 | Common:1; Rare:110 | ||||
chr5:139341687-139341979 | Common:1; Rare:79 | ||||
chr5:139342164-139342506 | Common:3; Rare:125 | ||||
chr5:139404069-139404330 | Common:1; Rare:67 | ||||
chr5:139439131-139439222 | Rare:17 | ||||
chr5:139439446-139439648 | Common:2; Rare:54 | ||||
chr5:139561066-139561415 | Common:1; Rare:140 |