Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:187547238-187547572 | Common:2; Rare:55 | ||||
chr2:190334564-190334734 | Rare:29 | ||||
chr2:200816943-200817248 | Rare:55 | ||||
chr2:202184707-202184809 | Rare:29 | ||||
chr2:202214355-202214568 | Common:1; Rare:40; Clinvar:1 | ||||
chr2:207935463-207935582 | Rare:18 | ||||
chr2:210540182-210540309 | Common:1; Rare:26 | ||||
chr2:210548932-210548965 | Rare:8 | ||||
chr2:210648449-210648793 | Common:2; Rare:67; Clinvar (benign):2 | ||||
chr2:218313485-218313742 | Rare:37 | ||||
chr2:218322244-218322369 | Rare:16 | ||||
chr2:218344452-218344828 | Common:1; Rare:112; Clinvar:4; Clinvar (benign):6 | ||||
chr2:218402645-218402714 | Rare:20 | ||||
chr2:218814383-218815115 | Rare:249; Clinvar:25; Clinvar (benign):5; Clinvar (pathogenic):17 | ||||
chr2:219224836-219225094 | Common:3; Rare:75 |