Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42964404-42964534 | Rare:61 | ||||
chr17:42980478-42980571 | Common:1; Rare:36 | ||||
chr17:43125466-43125654 | Rare:45; Clinvar (benign):1 | ||||
chr17:43170243-43170522 | Common:2; Rare:61 | ||||
chr17:43171016-43171274 | Common:1; Rare:87 | ||||
chr17:43833114-43833322 | Common:2; Rare:60 | ||||
chr17:43908179-43908453 | Common:1; Rare:45 | ||||
chr17:44070612-44070951 | Common:3; Rare:120; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44123571-44123844 | Common:3; Rare:79 | ||||
chr17:44170639-44170714 | Rare:15 | ||||
chr17:44186658-44187002 | Common:1; Rare:127 | ||||
chr17:44187171-44187274 | Rare:29 | ||||
chr17:44218997-44219170 | Rare:51 | ||||
chr17:44219917-44220209 | Common:5; Rare:94 | ||||
chr17:44221273-44221367 | Rare:30 |