| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:113532263-113532589 | Common:4; Rare:57 | ||||
| chr3:113674885-113674965 | Rare:26 | ||||
| chr3:113746104-113746348 | Common:1; Rare:95 | ||||
| chr3:113746744-113747102 | Common:4; Rare:79 | ||||
| chr3:114056481-114056857 | Common:2; Rare:137 | ||||
| chr3:114237553-114237590 | Common:2; Rare:6 | ||||
| chr3:114454685-114454997 | Common:4; Rare:31 | ||||
| chr3:114624176-114624407 | Common:1; Rare:46 | ||||
| chr3:114624925-114625041 | Common:1; Rare:16 | ||||
| chr3:115100182-115100404 | Rare:39 | ||||
| chr3:115147219-115147686 | Common:5; Rare:125 | ||||
| chr3:119240856-119241010 | Common:1; Rare:47 | ||||
| chr3:119294523-119294699 | Rare:35; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:119436924-119437033 | Rare:29 | ||||
| chr3:119463570-119463800 | Common:5; Rare:66 |