ID: 127888337 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:78086615-78087127 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80112816..80113328) | | |
ID: 127888336 | H3K4me1 hESC enhancer GRCh37_chr17:78083610-78084585 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80109811..80110786) | | |
ID: 127888335 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:78064021-78064580 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80090222..80090781) | | |
ID: 127888334 | H3K4me1 hESC enhancer GRCh37_chr17:78056255-78056756 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80082456..80082957) | | |
ID: 127888333 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:78039691-78040515 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80065892..80066716) | | |
ID: 127888332 | H3K4me1 hESC enhancer GRCh37_chr17:78018463-78018964 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80044664..80045165) | | |
ID: 127888331 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:78003463-78004332 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80029664..80030533) | | |
ID: 127888330 | H3K4me1 hESC enhancer GRCh37_chr17:77996703-77997568 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80022904..80023769) | | |
ID: 124904074 | uncharacterized LOC124904074 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80058266..80071536, complement) | | |
ID: 124904072 | uncharacterized LOC124904072 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80023900..80026104) | | |
ID: 121852954 | Sharpr-MPRA regulatory region 13982 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80037150..80037444) | | |
ID: 100616121 | microRNA 1268b [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80098828..80098877) | | |
ID: 125058 | TBC1 domain family member 16 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (79932343..80035872, complement) | | 616637 |
ID: 55036 | coiled-coil domain 40 molecular ruler complex subunit [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80036642..80100613) | CFAP172, CILD15, FAP172 | 613799 |
ID: 2548 | alpha glucosidase [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (80101581..80119881) | LYAG | 606800 |