Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:135497603-135497897 | Common:4; Rare:107; Clinvar:1; Clinvar (benign):2 | ||||
chr6:136289756-136290032 | Common:1; Rare:119 | ||||
chr6:136550394-136550701 | Common:2; Rare:88 | ||||
chr6:137219328-137219511 | Common:4; Rare:64; Clinvar (benign):2 | ||||
chr6:138773583-138773827 | Common:3; Rare:102 | ||||
chr6:139028628-139028813 | Common:1; Rare:37 | ||||
chr6:142147140-142147287 | Rare:54 | ||||
chr6:142301868-142302016 | Common:1; Rare:45 | ||||
chr6:143060724-143060919 | Common:7; Rare:67 | ||||
chr6:143450654-143450929 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
chr6:143843232-143843418 | Common:2; Rare:59 | ||||
chr6:144150449-144150529 | Common:1; Rare:21 | ||||
chr6:144285178-144285410 | Common:3; Rare:67 | ||||
chr6:145814685-145814921 | Common:1; Rare:111 | ||||
chr6:145964288-145964553 | Common:1; Rare:91 |