| ID: 127826671 | H3K27ac hESC enhancer GRCh37_chr13:95953650-95954424 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (95300987..95302170) | | |
| ID: 127826670 | H3K27ac hESC enhancer GRCh37_chr13:95856177-95856677 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (95203923..95204423) | | |
| ID: 127826669 | H3K4me1 hESC enhancer GRCh37_chr13:95845687-95846187 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (95193433..95193933) | | |
| ID: 127826668 | NANOG hESC enhancer GRCh37_chr13:95826697-95827198 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (95174443..95174944) | | |
| ID: 127826667 | OCT4-NANOG hESC enhancer GRCh37_chr13:95648475-95649263 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (94996221..94997009) | | |
| ID: 126861817 | BRD4-independent group 4 enhancer GRCh37_chr13:95861642-95862841 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (95209388..95210587) | | |
| ID: 124909511 | Sharpr-MPRA regulatory region 4491 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (95226595..95226889) | | |
| ID: 124903192 | uncharacterized LOC124903192 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (95278089..95281434) | | |
| ID: 109616987 | small nucleolar RNA, C/D box 13G [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (95210344..95210448) | | |
| ID: 106478987 | RNA, U6 small nuclear 62, pseudogene [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (95019235..95019336) | RNU6-62 | |
| ID: 106478985 | RNY3 pseudogene 8 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (95310833..95310895, complement) | | |
| ID: 102724149 | uncharacterized LOC102724149 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (95300951..95310874) | | |
| ID: 100873821 | RNY4 pseudogene 27 [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (95336109..95336199, complement) | | |
| ID: 10257 | ATP binding cassette subfamily C member 4 (PEL blood group) [Homo sapiens (human)] | Chromosome 13, NC_000013.11 (95019835..95301451, complement) | MOAT-B, MOATB, MRP4 | 605250 |