ID: 127896114 | H3K4me1 hESC enhancer GRCh37_chr22:37865281-37865782 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37469243..37469744) | | |
ID: 127896113 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:37863012-37863625 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37466974..37467587) | | |
ID: 127896112 | H3K4me1 hESC enhancer GRCh37_chr22:37816475-37817143 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37420436..37421105) | | |
ID: 127896111 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:37815805-37816474 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37419766..37420435) | | |
ID: 127896110 | H3K4me1 hESC enhancer GRCh37_chr22:37812286-37812830 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37416247..37416791) | | |
ID: 127896109 | H3K4me1 hESC enhancer GRCh37_chr22:37806589-37807090 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37410550..37411051) | | |
ID: 127896108 | H3K4me1 hESC enhancer GRCh37_chr22:37798615-37799363 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37402575..37403323) | | |
ID: 127896107 | H3K4me1 hESC enhancer GRCh37_chr22:37782078-37782616 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37386038..37386576) | | |
ID: 127896106 | H3K4me1 hESC enhancer GRCh37_chr22:37774300-37774868 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37378260..37378828) | | |
ID: 127896105 | H3K4me1 hESC enhancer GRCh37_chr22:37764078-37765044 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37368038..37369004) | | |
ID: 127896104 | H3K4me1 hESC enhancer GRCh37_chr22:37751415-37751915 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37355375..37355875) | | |
ID: 127896103 | H3K4me1 hESC enhancer GRCh37_chr22:37750914-37751414 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37354874..37355374) | | |
ID: 127896102 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:37725005-37725650 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37328964..37329609) | | |
ID: 126863143 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr22:37723358-37724557 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37327317..37328516) | | |
ID: 125446229 | Sharpr-MPRA regulatory region 3535 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37330508..37330802) | | |
ID: 124905114 | uncharacterized LOC124905114 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37380232..37382359) | | |
ID: 105373024 | uncharacterized LOC105373024 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37310621..37332136, complement) | | |
ID: 100506271 | uncharacterized LOC100506271 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37352190..37354839, complement) | | |
ID: 114794 | extracellular leucine rich repeat and fibronectin type III domain containing 2 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37340644..37427479, complement) | LRRC62, PPP1R29 | 620223 |
ID: 4242 | MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (37469063..37486384, complement) | | 602577 |