Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:17439326-17439412 | Common:1; Rare:11 | ||||
chr1:17439669-17439892 | Rare:76 | ||||
chr1:18107367-18107560 | Rare:37 | ||||
chr1:19210136-19210417 | Rare:105 | ||||
chr1:19251498-19251952 | Common:9; Rare:152 | ||||
chr1:19311943-19312333 | Common:8; Rare:178 | ||||
chr1:19596854-19597080 | Common:2; Rare:103 | ||||
chr1:20486191-20486357 | Rare:36 | ||||
chr1:20508045-20508236 | Common:2; Rare:68 | ||||
chr1:20552179-20552590 | Common:1; Rare:85 | ||||
chr1:20661340-20661709 | Common:3; Rare:133; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20787196-20787399 | Rare:102 | ||||
chr1:21176852-21177102 | Rare:71 | ||||
chr1:21345476-21345677 | Common:1; Rare:77 | ||||
chr1:21440037-21440167 | Rare:30 |