| ID: 128772425 | melanoma risk locus-associated MPRA allelic enhancer 20:62307938 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63676513..63676657) | | |
| ID: 127894270 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:62285437-62286115 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63654084..63654762) | | |
| ID: 127894269 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:62284757-62285436 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63653404..63654083) | | |
| ID: 127894268 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:62282910-62283480 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63651557..63652127) | | |
| ID: 127894267 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:62275446-62276015 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63644093..63644662) | | |
| ID: 127894266 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:62273358-62274096 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63641986..63642743) | | |
| ID: 127894265 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:62272271-62273029 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63640918..63641676) | | |
| ID: 127894264 | H3K4me1 hESC enhancer GRCh37_chr20:62269990-62270750 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63638637..63639397) | | |
| ID: 124904954 | uncharacterized LOC124904954 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63671356..63678375, complement) | | |
| ID: 114004357 | Sharpr-MPRA regulatory region 12780 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63648236..63648530) | | |
| ID: 100533107 | RTEL1-TNFRSF6B readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63657810..63698698) | | |
| ID: 100505771 | melanoma highly expressed competing endogenous lncRNA for miR-425 and miR-489 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63627235..63628824) | | |
| ID: 51750 | regulator of telomere elongation helicase 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63657810..63696253) | C20orf41, DKCA4, DKCB5, NHL, PFBMFT3, RTEL | 608833 |
| ID: 50861 | stathmin 3 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63639712..63653424, complement) | SCLIP | 608362 |