Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:127880797-127880956 | Rare:51 | ||||
chr4:128060979-128061325 | Common:1; Rare:125 | ||||
chr4:128811056-128811317 | Rare:53 | ||||
chr4:129093422-129093736 | Common:2; Rare:88 | ||||
chr4:138242236-138242646 | Common:1; Rare:86 | ||||
chr4:139301215-139301568 | Common:5; Rare:104 | ||||
chr4:139453653-139453712 | Common:1; Rare:23 | ||||
chr4:139453742-139454210 | Common:3; Rare:131; Clinvar:10; Clinvar (benign):4 | ||||
chr4:139556106-139556310 | Rare:52 | ||||
chr4:139556403-139556623 | Rare:31 | ||||
chr4:139556750-139556864 | Rare:18 | ||||
chr4:140373348-140373709 | Common:3; Rare:143 | ||||
chr4:142405394-142405545 | Rare:24 | ||||
chr4:143513349-143513759 | Common:2; Rare:130 | ||||
chr4:143513864-143514066 | Common:1; Rare:91 |