Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:129054884-129055226 | Common:2; Rare:66 | ||||
chr7:129611623-129611811 | Common:1; Rare:59 | ||||
chr7:130205399-130205525 | Rare:56 | ||||
chr7:131109922-131110109 | Common:1; Rare:28 | ||||
chr7:131327715-131327901 | Rare:65 | ||||
chr7:134646566-134646907 | Common:7; Rare:110 | ||||
chr7:135170486-135170832 | Common:3; Rare:125 | ||||
chr7:135662357-135662551 | Common:4; Rare:87 | ||||
chr7:138002013-138002268 | Common:1; Rare:67 | ||||
chr7:139109334-139109423 | Common:1; Rare:29 | ||||
chr7:139133671-139133833 | Rare:43 | ||||
chr7:139359761-139359997 | Common:3; Rare:81 | ||||
chr7:141014915-141015018 | Rare:25 | ||||
chr7:141551322-141551423 | Rare:32; Clinvar:4; Clinvar (benign):2 | ||||
chr7:141738058-141738614 | Common:5; Rare:160 |