Proximal
GM19238(Human) | 21581 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:109410363-109410528 | Common:1; Rare:52 | ||||
| chr5:109689200-109689509 | Common:6; Rare:138 | ||||
| chr5:109689745-109690113 | Common:3; Rare:133 | ||||
| chr5:110738608-110739092 | Common:3; Rare:143 | ||||
| chr5:110739226-110739586 | Common:4; Rare:132; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr5:111092183-111092467 | Common:2; Rare:141; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:111092684-111092843 | Rare:45 | ||||
| chr5:111223908-111224000 | Rare:22 | ||||
| chr5:111224180-111224526 | Rare:140 | ||||
| chr5:111512379-111512885 | Common:4; Rare:155 | ||||
| chr5:111512954-111513071 | Common:1; Rare:26 | ||||
| chr5:111757078-111757356 | Common:6; Rare:67 | ||||
| chr5:111757513-111757972 | Common:1; Rare:168 | ||||
| chr5:111757997-111758357 | Common:5; Rare:108 | ||||
| chr5:112707295-112707903 | Common:10; Rare:246; Clinvar:119; Clinvar (benign):21; Clinvar (pathogenic):1 |
- 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