Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19298092-19298125 | Rare:5 | ||||
chr1:19408545-19408715 | Common:2; Rare:32 | ||||
chr1:19626137-19626424 | Common:3; Rare:60 | ||||
chr1:19889173-19889464 | Common:2; Rare:50 | ||||
chr1:20032301-20032423 | Common:1; Rare:26 | ||||
chr1:20081738-20081909 | Rare:27 | ||||
chr1:20183003-20183099 | Rare:18 | ||||
chr1:20213364-20213479 | Common:1; Rare:16 | ||||
chr1:20428772-20428920 | Rare:24 | ||||
chr1:20601189-20601354 | Rare:29 | ||||
chr1:20650253-20650607 | Common:4; Rare:101; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:20654355-20654407 | Common:1; Rare:16; Clinvar (benign):1 | ||||
chr1:20655445-20655705 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):3 | ||||
chr1:20903620-20903737 | Rare:15 | ||||
chr1:21850151-21850310 | Common:2; Rare:47 |