Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40097234-40097286 | Rare:23; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:40161231-40161402 | Common:1; Rare:47 | ||||
chr1:40257903-40258265 | Common:4; Rare:98; Clinvar:7 | ||||
chr1:40374376-40374645 | Common:12; Rare:52 | ||||
chr1:40449983-40450174 | Common:3; Rare:75 | ||||
chr1:40508647-40508769 | Common:3; Rare:32 | ||||
chr1:40531470-40531715 | Rare:69 | ||||
chr1:40691504-40691805 | Common:2; Rare:147 | ||||
chr1:40692010-40692241 | Common:2; Rare:75 | ||||
chr1:40709154-40709369 | Rare:50 | ||||
chr1:40979583-40979739 | Common:2; Rare:58 | ||||
chr1:41242104-41242345 | Rare:70 | ||||
chr1:42335134-42335369 | Common:6; Rare:116 | ||||
chr1:42456439-42456590 | Rare:66 | ||||
chr1:42658271-42658455 | Common:2; Rare:53 |