Proximal
Caco-2(Human) | 27829 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50526397-50526502 | Common:2; Rare:43; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr22:50530271-50530548 | Common:1; Rare:101 | ||||
| chr22:50530895-50531239 | Common:2; Rare:126 | ||||
| chr22:50531608-50531794 | Common:2; Rare:40 | ||||
| chr22:50531813-50532016 | Rare:61 | ||||
| chr22:50532113-50532305 | Common:1; Rare:50 | ||||
| chr22:50562807-50563112 | Common:5; Rare:80 | ||||
| chr22:50582174-50582437 | Common:1; Rare:96; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:50582511-50582940 | Common:7; Rare:171; Clinvar:6; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr22:50582954-50583212 | Common:3; Rare:87 | ||||
| chr22:50600642-50600824 | Rare:48 | ||||
| chr22:50628145-50628352 | Common:7; Rare:90 | ||||
| chr22:50674803-50674962 | Common:1; Rare:52 | ||||
| chr22:50675067-50675261 | Rare:60; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50783585-50783823 | Common:2; Rare:82 |
- 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