ID: 132090639 | Neanderthal introgressed variant-containing enhancer experimental_63007 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21747001..21747170) | | |
ID: 130067039 | ATAC-STARR-seq lymphoblastoid active region 18710 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21767082..21767151) | | |
ID: 130067038 | ATAC-STARR-seq lymphoblastoid active region 18709 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21764722..21764771) | | |
ID: 130067037 | ATAC-STARR-seq lymphoblastoid active region 18708 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21764662..21764711) | | |
ID: 130067036 | ATAC-STARR-seq lymphoblastoid active region 18707 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21756515..21756614) | | |
ID: 130067035 | ATAC-STARR-seq lymphoblastoid active region 18706 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21755011..21755080) | | |
ID: 130067034 | ATAC-STARR-seq lymphoblastoid active region 18705 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21754501..21754630) | | |
ID: 130067033 | ATAC-STARR-seq lymphoblastoid silent region 13515 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21735513..21736362) | | |
ID: 130067032 | ATAC-STARR-seq lymphoblastoid silent region 13514 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21735443..21735492) | | |
ID: 130067031 | ATAC-STARR-seq lymphoblastoid active region 18704 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21713611..21713660) | | |
ID: 130067030 | ATAC-STARR-seq lymphoblastoid active region 18703 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21690309..21690418) | | |
ID: 130067029 | ATAC-STARR-seq lymphoblastoid active region 18702 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21688994..21689043) | | |
ID: 130067028 | ATAC-STARR-seq lymphoblastoid silent region 13513 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21657511..21657840) | | |
ID: 129664805 | ReSE screen-validated silencer GRCh37_chr22:22144051-22144194 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21789762..21789905) | | |
ID: 129664804 | ReSE screen-validated silencer GRCh37_chr22:22112788-22113234 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21758499..21758945) | | |
ID: 129664803 | ReSE screen-validated silencer GRCh37_chr22:22084296-22084483 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21730007..21730194) | | |
ID: 129664802 | ReSE screen-validated silencer GRCh37_chr22:22077940-22078170 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21723651..21723881) | | |
ID: 129664801 | ReSE screen-validated silencer GRCh37_chr22:22068158-22068316 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21713869..21714027) | | |
ID: 129664800 | ReSE screen-validated silencer GRCh37_chr22:22029290-22029497 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21675001..21675208) | | |
ID: 127895458 | H3K4me1 hESC enhancer GRCh37_chr22:22041165-22041665 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (21686876..21687376) | | |