Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:108654085-108654154 | Rare:11 | ||||
chr6:110876311-110876562 | Common:1; Rare:63 | ||||
chr6:111602093-111602158 | Rare:8 | ||||
chr6:111604294-111604390 | Rare:13 | ||||
chr6:111604449-111604685 | Common:2; Rare:39 | ||||
chr6:112154876-112155004 | Rare:35; Clinvar:1; Clinvar (benign):4 | ||||
chr6:112202632-112202811 | Common:5; Rare:27 | ||||
chr6:112203991-112204324 | Rare:43 | ||||
chr6:112218682-112218836 | Common:2; Rare:29 | ||||
chr6:112223092-112223247 | Rare:31 | ||||
chr6:112251517-112251662 | Rare:34 | ||||
chr6:116369656-116369848 | Common:3; Rare:33 | ||||
chr6:117578947-117579209 | Rare:55 | ||||
chr6:117999044-117999094 | Rare:17 | ||||
chr6:117999132-117999169 | Rare:9 |