| ID: 129662258 | ReSE screen-validated silencer GRCh37_chr8:23778915-23779185 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23921402..23921672) | | |
| ID: 127458961 | OCT4-NANOG hESC enhancer GRCh37_chr8:23836477-23837459 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23978964..23979946) | | |
| ID: 127458960 | OCT4-NANOG hESC enhancer GRCh37_chr8:23775841-23776377 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23918328..23918864) | | |
| ID: 127458959 | OCT4-NANOG hESC enhancer GRCh37_chr8:23775304-23775840 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23917791..23918327) | | |
| ID: 127458958 | H3K4me1 hESC enhancer GRCh37_chr8:23641595-23642178 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23784082..23784665) | | |
| ID: 126860328 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr8:23747587-23748786 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23890074..23891273) | | |
| ID: 126860327 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr8:23655625-23656824 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23798112..23799311) | | |
| ID: 124900262 | uncharacterized LOC124900262 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23806229..23806377, complement) | | |
| ID: 113788272 | Sharpr-MPRA regulatory region 10080 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (24039336..24039630) | | |
| ID: 113788271 | BRD4-independent group 4 enhancer GRCh37_chr8:23618596-23619795 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23761083..23762282) | | |
| ID: 107986931 | uncharacterized LOC107986931 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23917333..24207528) | | |
| ID: 107986930 | uncharacterized LOC107986930 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23663078..23802942) | | |
| ID: 106481635 | RNA, U1 small nuclear 148, pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (24076997..24077158, complement) | | |
| ID: 105379328 | uncharacterized LOC105379328 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (24089989..24106304) | | |
| ID: 101929258 | uncharacterized LOC101929258 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23712864..23726943, complement) | | |
| ID: 6781 | stanniocalcin 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (23841929..23854806, complement) | STC | 601185 |