Proximal
GM18507(Human) | 19257 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:123511913-123512341 | Common:3; Rare:131 | ||||
| chr5:124748363-124748486 | Rare:16 | ||||
| chr5:124748804-124749057 | Common:2; Rare:63 | ||||
| chr5:126423553-126423629 | Rare:29 | ||||
| chr5:126594977-126595363 | Common:5; Rare:159; Clinvar:12; Clinvar (benign):12; Clinvar (pathogenic):5 | ||||
| chr5:126600814-126601011 | Common:1; Rare:89 | ||||
| chr5:126601297-126601444 | Rare:55 | ||||
| chr5:126776587-126777232 | Common:5; Rare:212; Clinvar:6; Clinvar (benign):8 | ||||
| chr5:126777691-126777819 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr5:126777847-126778605 | Common:4; Rare:225 | ||||
| chr5:127030449-127030903 | Common:4; Rare:116 | ||||
| chr5:127030920-127030959 | Rare:8 | ||||
| chr5:127073364-127073627 | Common:5; Rare:97 | ||||
| chr5:127517495-127517784 | Common:7; Rare:116 | ||||
| chr5:127518089-127518152 | Common:1; Rare:15 |
- 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