ID: 127274241 | H3K4me1 hESC enhancer GRCh37_chr2:100871469-100871968 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (100255007..100255506) | | |
ID: 127274240 | OCT4-NANOG hESC enhancer GRCh37_chr2:100735506-100736449 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (100119044..100119987) | | |
ID: 127274239 | H3K27ac hESC enhancer GRCh37_chr2:100521553-100522052 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (99905091..99905590) | | |
ID: 127274238 | H3K4me1 hESC enhancer GRCh37_chr2:100218069-100218631 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (99601607..99602169) | | |
ID: 127274237 | NANOG hESC enhancer GRCh37_chr2:100188674-100189175 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (99572212..99572713) | | |
ID: 127274236 | NANOG hESC enhancer GRCh37_chr2:100171857-100172363 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (99555395..99555901) | | |
ID: 127274235 | H3K4me1 hESC enhancer GRCh37_chr2:100170926-100171473 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (99554464..99555011) | | |
ID: 127274234 | H3K4me1 hESC enhancer GRCh37_chr2:100170377-100170925 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (99553915..99554463) | | |
ID: 127274233 | H3K4me1 hESC enhancer GRCh37_chr2:100146131-100146758 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (99529669..99530296) | | |
ID: 127274232 | H3K27ac hESC enhancer GRCh37_chr2:100106417-100107302 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (99489852..99490840) | | |
ID: 126806283 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr2:100865373-100866572 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (100248911..100250110) | | |
ID: 126806282 | BRD4-independent group 4 enhancer GRCh37_chr2:100483776-100484975 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (99867314..99868513) | | |
ID: 124906051 | uncharacterized LOC124906051 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (99658050..99661816) | | |
ID: 120961774 | Sharpr-MPRA regulatory region 9249 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (100047027..100047321) | | |
ID: 109113861 | fragile site, folic acid type, rare, fra(2)(q11.2) [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (100104799..100104824) | | |
ID: 105373504 | uncharacterized LOC105373504 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (99692199..99701580) | | |
ID: 150577 | long intergenic non-protein coding RNA 1104 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (100208254..100251484) | | |
ID: 51455 | REV1 DNA directed polymerase [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (99400477..99490202, complement) | AIBP80L, REV1 | 606134 |
ID: 3899 | ALF transcription elongation factor 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (99545419..100142590, complement) | KINS, LAF4, MLLT2-like | 601464 |