| ID: 129660529 | ReSE screen-validated silencer GRCh37_chr1:231024325-231024499 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230888579..230888753) | | |
| ID: 129660528 | ReSE screen-validated silencer GRCh37_chr1:230914014-230914159 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230778268..230778413) | | |
| ID: 127271957 | H3K4me1 hESC enhancer GRCh37_chr1:231012987-231013486 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230877241..230877740) | | |
| ID: 127271956 | H3K4me1 hESC enhancer GRCh37_chr1:231012485-231012986 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230876739..230877240) | | |
| ID: 127271955 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:231004239-231004830 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230868450..230869084) | | |
| ID: 127271954 | NANOG hESC enhancer GRCh37_chr1:230919761-230920350 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230784015..230784604) | | |
| ID: 126806042 | MED14-independent group 3 enhancer GRCh37_chr1:230990988-230992187 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230855242..230856441) | | |
| ID: 124904548 | uncharacterized LOC124904548 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230824500..230833931) | | |
| ID: 124904547 | uncharacterized LOC124904547 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230878655..230890480, complement) | | |
| ID: 110121263 | VISTA enhancer hs2133 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230750693..230754328) | | |
| ID: 110121205 | VISTA enhancer hs1766 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230848777..230852235) | | |
| ID: 106480536 | RNA, 7SL, cytoplasmic 837, pseudogene [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230894141..230894427) | | |
| ID: 105373167 | uncharacterized LOC105373167 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230889400..230898221) | | |
| ID: 101927604 | uncharacterized LOC101927604 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230874846..230879015) | | |
| ID: 100873313 | RNA, 5S ribosomal pseudogene 79 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230820250..230820358) | RN5S79 | |
| ID: 84886 | chromosome 1 open reading frame 198 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230837119..230869591, complement) | | |
| ID: 10753 | calpain 9 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (230747388..230801989) | GC36, nCL-4 | 606401 |