Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42852448-42852472 | Common:1; Rare:8 | ||||
chr17:42964428-42964528 | Rare:49 | ||||
chr17:42998388-42998479 | Common:3; Rare:36 | ||||
chr17:43170284-43170397 | Rare:21 | ||||
chr17:43170414-43170712 | Common:2; Rare:57 | ||||
chr17:43171024-43171251 | Rare:70 | ||||
chr17:43211750-43211903 | Common:1; Rare:34 | ||||
chr17:43398917-43398996 | Rare:19 | ||||
chr17:44070619-44070930 | Common:3; Rare:107; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44093726-44093970 | Common:1; Rare:49 | ||||
chr17:44170608-44170725 | Rare:25 | ||||
chr17:44186658-44187002 | Common:1; Rare:127 | ||||
chr17:44209375-44209677 | Rare:76 | ||||
chr17:44220845-44221071 | Rare:72 | ||||
chr17:44345067-44345321 | Rare:52; Clinvar:5; Clinvar (benign):3 |