| ID: 129932769 | ATAC-STARR-seq lymphoblastoid active region 2730 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231420843..231421112) | | |
| ID: 129932768 | ATAC-STARR-seq lymphoblastoid active region 2729 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231377109..231377168) | | |
| ID: 129660532 | ReSE screen-validated silencer GRCh37_chr1:231634962-231635134 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231499216..231499388) | | |
| ID: 129660531 | ReSE screen-validated silencer GRCh37_chr1:231558174-231558498 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231421493..231422752) | | |
| ID: 129660530 | ReSE screen-validated silencer GRCh37_chr1:231538414-231538617 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231402668..231402871) | | |
| ID: 127271970 | NANOG hESC enhancer GRCh37_chr1:231614566-231615067 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231478820..231479321) | | |
| ID: 127271969 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:231474651-231475525 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231338905..231339779) | | |
| ID: 127271968 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:231473776-231474650 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231338030..231338904) | | |
| ID: 126806044 | MED14-independent group 3 enhancer GRCh37_chr1:231663972-231665171 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231527936..231529425) | | |
| ID: 126806043 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:231647424-231648623 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231511678..231512877) | | |
| ID: 122526782 | TSNAX divergent transcript [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231520734..231528556, complement) | | |
| ID: 122152337 | Sharpr-MPRA regulatory region 8140 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231525963..231526257) | | |
| ID: 122152336 | Sharpr-MPRA regulatory region 11665 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231393823..231394117) | | |
| ID: 107985360 | uncharacterized LOC107985360 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231357290..231369843) | | |
| ID: 100303453 | TSNAX-DISC1 readthrough (NMD candidate) [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231528653..232041272) | | |
| ID: 645339 | small nuclear ribonucleoprotein D2 pseudogene 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231475762..231476525, complement) | | |
| ID: 83932 | SprT-like N-terminal domain [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231338293..231355023) | C1orf124, DVC1, PRO4323, spartan | 616086 |
| ID: 54583 | egl-9 family hypoxia inducible factor 1 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231363756..231422287, complement) | C1orf12, ECYT3, HALAH, HIF-PH2, HIFPH2, HPH-2, HPH2, PHD2, SM20, ZMYND6 | 606425 |
| ID: 7257 | translin associated factor X [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (231528669..231566524) | C3PO, TRAX | 602964 |