Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:26221787-26222010 | Rare:67 | ||||
chr13:26557449-26557782 | Common:4; Rare:134 | ||||
chr13:27251225-27251617 | Common:8; Rare:122 | ||||
chr13:27270696-27270831 | Rare:44 | ||||
chr13:27424536-27424723 | Common:2; Rare:58 | ||||
chr13:27450037-27450222 | Common:3; Rare:57 | ||||
chr13:27450519-27450643 | Common:2; Rare:53 | ||||
chr13:27620461-27620818 | Common:2; Rare:119 | ||||
chr13:28138137-28138234 | Common:1; Rare:28 | ||||
chr13:28659049-28659180 | Rare:58; Clinvar (pathogenic):1 | ||||
chr13:28718814-28719009 | Rare:57 | ||||
chr13:29850121-29850362 | Common:1; Rare:71 | ||||
chr13:30306987-30307227 | Common:5; Rare:64 | ||||
chr13:30307372-30307604 | Common:2; Rare:78 | ||||
chr13:30616945-30617151 | Rare:40 |