Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:70688182-70688632 | Common:2; Rare:115 | ||||
chr4:70704131-70704257 | Rare:28 | ||||
chr4:70721767-70722135 | Common:2; Rare:48 | ||||
chr4:70722452-70722708 | Rare:48 | ||||
chr4:70839232-70839442 | Common:2; Rare:92 | ||||
chr4:70902131-70902478 | Common:6; Rare:120 | ||||
chr4:70993482-70993822 | Common:5; Rare:101 | ||||
chr4:71187055-71187339 | Common:1; Rare:88 | ||||
chr4:73069435-73069499 | Rare:28; Clinvar (benign):1 | ||||
chr4:73069642-73069947 | Common:1; Rare:138 | ||||
chr4:73258505-73258943 | Common:1; Rare:136 | ||||
chr4:73259100-73259289 | Common:1; Rare:52 | ||||
chr4:74157918-74158023 | Common:1; Rare:44 | ||||
chr4:74158031-74158234 | Rare:97 | ||||
chr4:75514268-75514793 | Common:1; Rare:164 |