Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:217631020-217631375 | Common:2; Rare:98 | ||||
chr1:218285178-218285449 | Common:4; Rare:111 | ||||
chr1:218346842-218346963 | Rare:33; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:219173506-219173900 | Common:1; Rare:113 | ||||
chr1:219174032-219174212 | Rare:34 | ||||
chr1:220272318-220272573 | Rare:73; Clinvar:5 | ||||
chr1:220879221-220879759 | Common:11; Rare:139 | ||||
chr1:220881421-220881537 | Rare:25 | ||||
chr1:221742048-221742288 | Rare:61 | ||||
chr1:222589874-222589965 | Common:1; Rare:22 | ||||
chr1:222644095-222644407 | Common:3; Rare:92 | ||||
chr1:222712437-222712854 | Common:3; Rare:145 | ||||
chr1:222713230-222713408 | Common:1; Rare:54 | ||||
chr1:223143219-223143368 | Common:3; Rare:43 | ||||
chr1:224183111-224183289 | Common:2; Rare:85 |