| ID: 127886409 | H3K4me1 hESC enhancer GRCh37_chr17:28549461-28549976 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30222443..30222958) | | |
| ID: 127886408 | H3K4me1 hESC enhancer GRCh37_chr17:28468415-28468916 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30141397..30141898) | | |
| ID: 126862529 | BRD4-independent group 4 enhancer GRCh37_chr17:28443345-28444544 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30116327..30117526) | | |
| ID: 124903970 | uncharacterized LOC124903970 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30203002..30206512) | | |
| ID: 110806307 | serotonin transporter intronic VNTR enhancer [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30221317..30221615) | 5HTT-VNTR2, 5HTTVNTR, STin2.10, STin2.12, STin2.9, VNTR2 | |
| ID: 110806262 | solute carrier family 6 member 4 gene promoter [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30235481..30237521) | | |
| ID: 105371720 | uncharacterized LOC105371720 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30236791..30252233) | | |
| ID: 100423003 | microRNA 3184 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30117086..30117160, complement) | | |
| ID: 100418889 | syntaxin 18 pseudogene 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30068569..30069800) | | |
| ID: 100379296 | RNY4 pseudogene 13 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30059054..30059147, complement) | | |
| ID: 494335 | microRNA 423 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30117079..30117172) | MIRN423, hsa-mir-423, mir-423 | |
| ID: 374786 | EF-hand calcium binding domain 5 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (29929903..30108452) | | |
| ID: 84081 | nuclear speckle splicing regulatory protein 1 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30116816..30186475) | CCDC55, HSPC095, NEDSSBA, NSrp70 | 616173 |
| ID: 6532 | solute carrier family 6 member 4 [Homo sapiens (human)] | Chromosome 17, NC_000017.11 (30194319..30235697, complement) | 5-HTT, 5-HTTLPR, 5HTT, HTT, OCD1, SERT, SERT1, hSERT | 182138 |