Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156751347-156751608 | Rare:63 | ||||
chr1:156767427-156767611 | Rare:53 | ||||
chr1:157138322-157138424 | Common:1; Rare:24 | ||||
chr1:159924574-159924716 | Rare:36 | ||||
chr1:160190290-160190795 | Common:3; Rare:120 | ||||
chr1:160190863-160191021 | Common:2; Rare:56; Clinvar:1 | ||||
chr1:160261638-160261786 | Common:1; Rare:32 | ||||
chr1:160261906-160262303 | Rare:98 | ||||
chr1:160262327-160262644 | Common:1; Rare:90 | ||||
chr1:160343173-160343410 | Rare:94 | ||||
chr1:161045887-161046052 | Common:1; Rare:44 | ||||
chr1:161117953-161118141 | Rare:92 | ||||
chr1:161132424-161132862 | Common:2; Rare:139 | ||||
chr1:161166268-161166521 | Common:2; Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161199052-161199304 | Rare:41 |