| ID: 127887088 | H3K4me1 hESC enhancer GRCh37_chr17:43513205-43513858 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45435839..45436492) | | |
| ID: 127887087 | H3K4me1 hESC enhancer GRCh37_chr17:43507521-43508021 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45430155..45430655) | | |
| ID: 127887086 | H3K4me1 hESC enhancer GRCh37_chr17:43507020-43507520 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45429654..45430154) | | |
| ID: 127887085 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:43502838-43503408 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45425472..45426042) | | |
| ID: 127887084 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:43501589-43502093 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45424223..45424727) | | |
| ID: 127887083 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:43501082-43501588 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45423716..45424222) | | |
| ID: 127887082 | H3K4me1 hESC enhancer GRCh37_chr17:43488992-43489492 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45411626..45412156) | | |
| ID: 127887081 | H3K4me1 hESC enhancer GRCh37_chr17:43471827-43472486 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45394461..45395120) | | |
| ID: 127887080 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:43462245-43463212 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45384879..45385846) | | |
| ID: 127887079 | H3K27ac hESC enhancer GRCh37_chr17:43453675-43454480 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45376309..45377114) | | |
| ID: 124904016 | uncharacterized LOC124904016 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45428563..45429349) | | |
| ID: 100423004 | microRNA 4315-1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45475363..45475435, complement) | | |
| ID: 201176 | Rho GTPase activating protein 27 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45393908..45432870, complement) | CAMGAP1, PP905, SH3D20, SH3P20 | 610591 |
| ID: 9842 | pleckstrin homology and RUN domain containing M1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (45434209..45490721, complement) | AP162, B2, OPTA3, OPTB6 | 611466 |