Proximal
GM18507(Human) | 19257 records | Show included studies| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:110738613-110739195 | Common:3; Rare:182; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:110739398-110739552 | Common:1; Rare:49 | ||||
| chr5:111092195-111092426 | Common:2; Rare:118; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:111224185-111224314 | Rare:39 | ||||
| chr5:111512389-111512820 | Common:4; Rare:145 | ||||
| chr5:111513022-111513072 | Common:1; Rare:10 | ||||
| chr5:111757064-111757395 | Common:6; Rare:83 | ||||
| chr5:111757547-111757604 | Rare:14 | ||||
| chr5:111757781-111758129 | Common:2; Rare:122 | ||||
| chr5:111758133-111758299 | Common:3; Rare:41 | ||||
| chr5:112707329-112707813 | Common:9; Rare:198; Clinvar:95; Clinvar (benign):19; Clinvar (pathogenic):1 | ||||
| chr5:112707818-112707893 | Rare:33; Clinvar:18 | ||||
| chr5:112737717-112737962 | Rare:60; Clinvar:3; Clinvar (benign):4 | ||||
| chr5:112861049-112861381 | Common:4; Rare:121 | ||||
| chr5:112861500-112861559 | Rare:19 |
- 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