| ID: 127271974 | NANOG hESC enhancer GRCh37_chr1:232173754-232174300 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (232038008..232038554) | | |
| ID: 127271973 | NANOG hESC enhancer GRCh37_chr1:231967105-231967615 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231831359..231831869) | | |
| ID: 127271972 | H3K4me1 hESC enhancer GRCh37_chr1:231787555-231788055 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231651809..231652309) | | |
| ID: 127271971 | H3K4me1 hESC enhancer GRCh37_chr1:231787054-231787554 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231651308..231651808) | | |
| ID: 126806045 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:232179763-232180962 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (232044017..232045588) | | |
| ID: 126806044 | MED14-independent group 3 enhancer GRCh37_chr1:231663972-231665171 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231527936..231529425) | | |
| ID: 124904549 | uncharacterized LOC124904549 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (232026566..232034876) | | |
| ID: 105373172 | uncharacterized LOC105373172 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (232042641..232058744) | | |
| ID: 105373171 | uncharacterized LOC105373171 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (232058828..232091925) | | |
| ID: 105373170 | uncharacterized LOC105373170 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231805575..231847703, complement) | | |
| ID: 104472714 | DISC1 intronic transcript 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231925834..231945205) | | |
| ID: 100873835 | RNA, U5A small nuclear 5, pseudogene [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231670635..231670750) | | |
| ID: 100303453 | TSNAX-DISC1 readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231528653..232041272) | | |
| ID: 100287814 | long intergenic non-protein coding RNA 582 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231591292..231612090, complement) | SMILO | |
| ID: 27185 | DISC1 scaffold protein [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231626790..232041272) | C1orf136, SCZD9 | 605210 |
| ID: 27184 | disrupted in schizophrenia 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231814626..231818517, complement) | DISC1-AS1, DISC1OS, NCRNA00015 | 606271 |
| ID: 7257 | translin associated factor X [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231528669..231566524) | C3PO, TRAX | 602964 |