ID: 132090901 | Neanderthal introgressed variant-containing enhancer experimental_50709 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79747410..79747579) | | |
ID: 130062791 | ATAC-STARR-seq lymphoblastoid silent region 9583 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79952135..79952184) | | |
ID: 130062790 | ATAC-STARR-seq lymphoblastoid silent region 9582 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79951495..79952004) | | |
ID: 130062789 | ATAC-STARR-seq lymphoblastoid silent region 9581 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79951095..79951174) | | |
ID: 130062788 | ATAC-STARR-seq lymphoblastoid silent region 9580 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79950935..79951054) | | |
ID: 130062787 | ATAC-STARR-seq lymphoblastoid silent region 9579 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79944265..79944324) | | |
ID: 130062786 | ATAC-STARR-seq lymphoblastoid silent region 9578 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79855190..79855269) | | |
ID: 130062785 | ATAC-STARR-seq lymphoblastoid active region 13545 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79819898..79820037) | | |
ID: 129664279 | ReSE screen-validated silencer GRCh37_chr18:77471187-77471379 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79711187..79711379) | | |
ID: 127889745 | H3K4me1 hESC enhancer GRCh37_chr18:77672372-77673288 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79912372..79913288) | | |
ID: 127889744 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr18:77664167-77664802 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79904167..79904802) | | |
ID: 127889743 | H3K4me1 hESC enhancer GRCh37_chr18:77601626-77602126 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79841626..79842126) | | |
ID: 127889742 | H3K4me1 hESC enhancer GRCh37_chr18:77577021-77577520 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79817021..79817520) | | |
ID: 127889741 | H3K4me1 hESC enhancer GRCh37_chr18:77576519-77577020 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79816519..79817020) | | |
ID: 127889740 | H3K4me1 hESC enhancer GRCh37_chr18:77557221-77557817 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79797221..79797988) | | |
ID: 127889739 | H3K4me1 hESC enhancer GRCh37_chr18:77458305-77458804 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79698305..79698804) | | |
ID: 127889738 | H3K4me1 hESC enhancer GRCh37_chr18:77457803-77458304 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79697803..79698304) | | |
ID: 127889737 | H3K4me1 hESC enhancer GRCh37_chr18:77442069-77442575 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79682069..79682575) | | |
ID: 127889736 | H3K4me1 hESC enhancer GRCh37_chr18:77441560-77442068 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79681560..79682068) | | |
ID: 127889735 | H3K27ac hESC enhancer GRCh37_chr18:77439436-77439944 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79679436..79679944) | | |