Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26900441-26900524 | Rare:32 | ||||
chr1:27725758-27725985 | Common:2; Rare:57 | ||||
chr1:28328902-28329064 | Common:1; Rare:49 | ||||
chr1:28505815-28506050 | Common:2; Rare:91 | ||||
chr1:28552862-28553140 | Common:2; Rare:110 | ||||
chr1:28643022-28643222 | Rare:77 | ||||
chr1:28736744-28737026 | Common:1; Rare:101 | ||||
chr1:29181819-29182143 | Common:2; Rare:123 | ||||
chr1:31296720-31297090 | Common:5; Rare:127 | ||||
chr1:31372983-31373320 | Common:2; Rare:96 | ||||
chr1:32200498-32200701 | Rare:45 | ||||
chr1:32291994-32292157 | Rare:63 | ||||
chr1:32394403-32394705 | Common:1; Rare:85 | ||||
chr1:32650917-32651309 | Common:2; Rare:149 | ||||
chr1:32817302-32817699 | Common:1; Rare:103; Clinvar:5; Clinvar (benign):2 |