| ID: 130006688 | ATAC-STARR-seq lymphoblastoid silent region 3873 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107858603..107858912) | | |
| ID: 130006687 | ATAC-STARR-seq lymphoblastoid active region 5475 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107858313..107858382) | | |
| ID: 130006686 | ATAC-STARR-seq lymphoblastoid silent region 3872 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107841927..107841986) | | |
| ID: 129663033 | ReSE screen-validated silencer GRCh37_chr11:107753920-107754108 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107883194..107883382) | | |
| ID: 129663032 | ReSE screen-validated silencer GRCh37_chr11:107661301-107661510 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107790575..107790784) | | |
| ID: 127822475 | NANOG-H3K4me1 hESC enhancer GRCh37_chr11:107704035-107704580 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107833309..107833854) | | |
| ID: 127822474 | H3K4me1 hESC enhancer GRCh37_chr11:107703489-107704034 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107832763..107833308) | | |
| ID: 127822473 | H3K4me1 hESC enhancer GRCh37_chr11:107702943-107703488 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107832217..107832762) | | |
| ID: 127822472 | H3K4me1 hESC enhancer GRCh37_chr11:107696193-107696692 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107825467..107825966) | | |
| ID: 127822471 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr11:107620738-107621281 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107750012..107750555) | | |
| ID: 127822470 | H3K4me1 hESC enhancer GRCh37_chr11:107612353-107612853 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107741627..107742127) | | |
| ID: 127822469 | H3K4me1 hESC enhancer GRCh37_chr11:107611852-107612352 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107741126..107741626) | | |
| ID: 127822468 | OCT4-NANOG hESC enhancer GRCh37_chr11:107578451-107579242 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107707725..107708516) | | |
| ID: 126861330 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr11:107710907-107712106 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107840181..107841380) | | |
| ID: 124902747 | uncharacterized LOC124902747 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107912589..107923223) | | |
| ID: 124902746 | uncharacterized LOC124902746 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107859230..107860989) | | |
| ID: 643949 | ribosomal protein lateral stalk subunit P2 pseudogene 3 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107908347..107908802) | RPLP2_2_1170 | |
| ID: 203930 | sorting nexin 7 pseudogene [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107735966..107738761, complement) | | |
| ID: 54733 | solute carrier family 35 member F2 [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107790991..107858787, complement) | HSNOV1 | 620350 |
| ID: 6588 | sarcolipin [Homo sapiens (human)] | Chromosome 11, NC_000011.10 (107707378..107712056, complement) | | 602203 |