Proximal
GM19238(Human) | 21581 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:83012802-83013341 | Common:2; Rare:135 | ||||
| chr4:83034388-83034476 | Rare:14 | ||||
| chr4:83034599-83034679 | Common:3; Rare:17 | ||||
| chr4:83034716-83035262 | Common:3; Rare:133 | ||||
| chr4:83035353-83035504 | Rare:25 | ||||
| chr4:83109678-83109758 | Common:1; Rare:17 | ||||
| chr4:83109828-83110364 | Common:3; Rare:117 | ||||
| chr4:83114646-83114807 | Common:2; Rare:34 | ||||
| chr4:83284404-83284648 | Common:2; Rare:95; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr4:83284658-83284901 | Common:3; Rare:98; Clinvar:1; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr4:83334751-83335026 | Rare:64 | ||||
| chr4:83455452-83455657 | Rare:91 | ||||
| chr4:83455729-83456176 | Common:3; Rare:179 | ||||
| chr4:83485000-83485383 | Common:4; Rare:157; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:83535637-83535784 | Rare:27 |
- Legend for epigenomic status:
- : Enriched for H3K27ac and DNaseI signal
- : Enriched for H3K4me3 and DNaseI signal
- : Enriched for CTCF binding signal
- Legend for core promoter element:
- : Found Initiator
- : Found DPR
- : Enriched TATA box