Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:99284532-99284807 | Common:2; Rare:88 | ||||
chr4:118265556-118265627 | Rare:26 | ||||
chr4:118265827-118265917 | Common:2; Rare:26 | ||||
chr4:118278507-118278769 | Common:4; Rare:96 | ||||
chr4:118591667-118591869 | Rare:83 | ||||
chr4:119454556-119454904 | Common:16; Rare:118 | ||||
chr4:125314863-125315212 | Common:4; Rare:92 | ||||
chr4:139028345-139028601 | Common:2; Rare:55 | ||||
chr4:139177898-139178127 | Rare:69 | ||||
chr4:140642029-140642090 | Rare:19 | ||||
chr4:141332592-141332936 | Common:1; Rare:89 | ||||
chr4:143348297-143348545 | Rare:43 | ||||
chr4:143559421-143559487 | Common:1; Rare:19 | ||||
chr4:143879908-143880007 | Rare:13 | ||||
chr4:143880435-143880699 | Common:4; Rare:78; Clinvar (benign):1 |