ID: 130061231 | ATAC-STARR-seq lymphoblastoid silent region 8744 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (57085003..57085582) | | |
ID: 130061230 | ATAC-STARR-seq lymphoblastoid active region 12425 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (57084703..57084782) | | |
ID: 130061229 | ATAC-STARR-seq lymphoblastoid silent region 8743 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (56978014..56978073) | | |
ID: 130061228 | ATAC-STARR-seq lymphoblastoid silent region 8742 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (56960652..56960761) | | |
ID: 129390897 | MPRA-validated peak2908 silencer [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (57027895..57028095) | | |
ID: 127887391 | NANOG-H3K4me1 hESC enhancer GRCh37_chr17:55156412-55157150 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (57079051..57079789) | | |
ID: 127887390 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:55123409-55124336 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (57046048..57046975) | | |
ID: 127887389 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:55095129-55095953 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (57017768..57018592) | | |
ID: 127887388 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:55094302-55095128 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (57016941..57017767) | | |
ID: 127887387 | OCT4-NANOG hESC enhancer GRCh37_chr17:55087342-55087971 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (57009981..57010610) | | |
ID: 125177516 | Sharpr-MPRA regulatory region 8860 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (57016108..57016402) | | |
ID: 119139901 | AKAP1 divergent transcript [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (57078294..57085038, complement) | | |
ID: 112533652 | Sharpr-MPRA regulatory region 7909 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (56960888..56961182) | | |
ID: 105371836 | uncharacterized LOC105371836 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (56961148..56976007) | | |
ID: 100419768 | ribosomal protein S15a pseudogene [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (56951648..56952443) | | |
ID: 376412 | ring finger protein 126 pseudogene 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (57045478..57046795) | | |
ID: 59342 | serine carboxypeptidase 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (56978131..57006768) | HSCP1, RISC | 619723 |
ID: 8161 | coilin [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (56938199..56961050, complement) | CLN80, p80-coilin | 600272 |