| ID: 127887567 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:60902506-60903242 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (62825145..62825881) | | |
| ID: 127887566 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:60839581-60840107 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (62762220..62762746) | | |
| ID: 127887565 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr17:60839055-60839580 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (62761694..62762219) | | |
| ID: 127887564 | H3K4me1 hESC enhancer GRCh37_chr17:60827764-60828372 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (62750403..62751011) | | |
| ID: 127887563 | H3K4me1 hESC enhancer GRCh37_chr17:60827154-60827763 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (62749793..62750402) | | |
| ID: 127887562 | NANOG-H3K4me1 hESC enhancer GRCh37_chr17:60817295-60817950 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (62739934..62740589) | | |
| ID: 127887561 | OCT4-NANOG hESC enhancer GRCh37_chr17:60782895-60783686 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (62705534..62706325) | | |
| ID: 127887560 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:60769963-60770624 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (62692602..62693263) | | |
| ID: 127887559 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:60769301-60769962 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (62691940..62692601) | | |
| ID: 105371855 | uncharacterized LOC105371855 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (62706206..62737922) | | |
| ID: 101927877 | MARCHF10 divergent transcript [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (62808502..62836371) | MARCH10-DT | |
| ID: 100128712 | PRELI domain containing 3B pseudogene 3 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (62841058..62841835) | SLMO2P3 | |
| ID: 162333 | membrane associated ring-CH-type finger 10 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (62701314..62808314, complement) | MARCH-X, MARCH10, RNF190 | 613337 |
| ID: 9902 | mannose receptor C-type 2 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (62627670..62693597) | CD280, CLEC13E, ENDO180, UPARAP | 612264 |