Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:127266785-127266893 | Common:1; Rare:41 | ||||
chr6:127343337-127343411 | Rare:11 | ||||
chr6:128520545-128520791 | Common:1; Rare:88 | ||||
chr6:132401428-132401595 | Common:1; Rare:50 | ||||
chr6:133953047-133953255 | Common:2; Rare:67 | ||||
chr6:134174834-134175105 | Common:1; Rare:130 | ||||
chr6:135054784-135054911 | Common:3; Rare:35 | ||||
chr6:135497609-135497810 | Common:4; Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
chr6:136289756-136290032 | Common:1; Rare:119 | ||||
chr6:136550414-136550687 | Common:2; Rare:75 | ||||
chr6:138773646-138773795 | Common:1; Rare:67 | ||||
chr6:139028628-139028832 | Common:1; Rare:42 | ||||
chr6:139029049-139029146 | Common:3; Rare:19 | ||||
chr6:139374435-139374764 | Common:3; Rare:135 | ||||
chr6:142301790-142302138 | Common:8; Rare:102 |