Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:79838832-79839055 | Rare:50 | ||||
chr17:79839393-79839686 | Rare:81 | ||||
chr17:80035869-80035988 | Common:1; Rare:40 | ||||
chr17:80101387-80101668 | Common:5; Rare:128; Clinvar (benign):5 | ||||
chr17:80147014-80147476 | Common:8; Rare:185 | ||||
chr17:80147520-80147599 | Rare:13 | ||||
chr17:80219642-80219649 | Rare:1 | ||||
chr17:80220273-80220457 | Rare:76; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr17:80260382-80260989 | Common:12; Rare:101 | ||||
chr17:80260992-80261100 | Rare:29 | ||||
chr17:80415088-80415233 | Common:1; Rare:103 | ||||
chr17:80415347-80415575 | Common:4; Rare:87 | ||||
chr17:80544718-80544956 | Common:2; Rare:61 | ||||
chr17:80991616-80991638 | Rare:2 | ||||
chr17:80991687-80991919 | Common:2; Rare:80 |