| ID: 130066134 | ATAC-STARR-seq lymphoblastoid active region 18086 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50350455..50350504) | | |
| ID: 130066133 | ATAC-STARR-seq lymphoblastoid active region 18085 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50339114..50339313) | | |
| ID: 130066132 | ATAC-STARR-seq lymphoblastoid silent region 13019 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50285867..50285916) | | |
| ID: 129664646 | ReSE screen-validated silencer GRCh37_chr20:48971862-48972074 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50355325..50355537) | | |
| ID: 129391189 | MPRA-validated peak4248 silencer [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50262218..50262418) | | |
| ID: 127893662 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:48938632-48939216 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50322095..50322679) | | |
| ID: 127893661 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:48938046-48938631 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50321509..50322094) | | |
| ID: 127893660 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:48937461-48938045 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50320924..50321508) | | |
| ID: 127893659 | H3K4me1 hESC enhancer GRCh37_chr20:48925583-48926093 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50309046..50309556) | | |
| ID: 127893658 | H3K4me1 hESC enhancer GRCh37_chr20:48925071-48925582 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50308534..50309045) | | |
| ID: 127893657 | H3K4me1 hESC enhancer GRCh37_chr20:48921517-48922292 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50304980..50305755) | | |
| ID: 127893656 | H3K4me1 hESC enhancer GRCh37_chr20:48910660-48911160 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50294123..50294623) | | |
| ID: 127893655 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:48908810-48909546 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50292273..50293009) | | |
| ID: 127893654 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:48894009-48894546 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50277472..50278009) | | |
| ID: 127893653 | H3K4me1 hESC enhancer GRCh37_chr20:48891665-48892164 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50275128..50275627) | | |
| ID: 127893652 | H3K4me1 hESC enhancer GRCh37_chr20:48891163-48891664 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50274626..50275127) | | |
| ID: 125387293 | Sharpr-MPRA regulatory region 5066 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50306052..50306346) | | |
| ID: 121627908 | Sharpr-MPRA regulatory region 10045 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50279012..50279306) | | |
| ID: 107985386 | uncharacterized LOC107985386 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50238454..50247491, complement) | | |
| ID: 105372657 | uncharacterized LOC105372657 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (50350698..50368866) | | |