Tag | Content |
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EnhancerAtlas ID | HS127-05771 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr11:66368020-66369440 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr11:66368781-66368796 | TGAACTCCTGACCTC | - | 6.22 | ZNF263 | MA0528.1 | chr11:66369022-66369043 | CTTTCTCCCCTCCCCTCCCCT | - | 6.27 | ZNF263 | MA0528.1 | chr11:66369017-66369038 | TTTTCCTTTCTCCCCTCCCCT | - | 6.3 | ZNF263 | MA0528.1 | chr11:66369027-66369048 | TCCCCTCCCCTCCCCTCCCCT | - | 6.91 | ZNF263 | MA0528.1 | chr11:66369034-66369055 | CCCTCCCCTCCCCTCTCCTTT | - | 6.91 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_10115 | chr11:66367594-66368803 | CD14 |
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| Number: 2 | ID | Chromosome | Start | End |
GH11I066600 | chr11 | 66367595 | 66368803 | GH11I066601 | chr11 | 66369061 | 66370282 |
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Enhancer Sequence | GTAAGTGTCT GTCTGGGTTT GGGCTTGGGC TGAGAGAGGA CCCAAAGTCT CAGAGGCAGG 60 GCAGGCAGCT CTTGGGATCA TAACAGTGTG ATTCCTTTTT GGTGGAGTCT TTTCCTCTCA 120 TTTTATTTTG CTGAGTTTGG AAACATTTGT TGACACTTTC TGTGATCAAG GCCCAGGGGA 180 TACAATAGAT TACAGCCCCA GTGCCTGACC CAAGGAGCAC ACAGTCTCTG GGGGAGATTA 240 CTGAATTCCA TGGTTTCCAG GCAGTGAGAT CATCCTTGCA GGAGCCTGCA AGAGGTCCTG 300 GAGCCCACAG TGAATAGTTC ATCTGCCTGA GGGGCAGGGG CAGTGGGAGG AAGTGAAATA 360 TGGAAGTTGA GGGTTTTACC TAAACTGAAA AGGCTGTCCC TGGTGTTCCC TAACACCCCG 420 GTCCTGGAGT TTCATTTTTC AGCAGAGAAT CATTTCCCAA TCTTCAGGGA ATTGTGTGTT 480 GCCTTAATGA TTTTTGCCTT ATCTGAGTAC TAGTTGTATT TTTAGTTACT CAATCATTTG 540 GTTTTTTTAT TTTATTTTCT GAGATGGAGT TTTGTTCTTA TTGCCCAGGC TAGAGTGCAA 600 TGGCGCAGTC CCAGCTCATT GCAACCTCCG CCTCCCAAGT TCAAACGATT CTCCTGCCTC 660 AGCCTCCCTA ATAGCTGGGA CTACAGGTGC ACACCACCAC ACCCGGGTAA TTTTTGTATT 720 TTTAGTAGAG ATGGGGTTTC ACCAGGTTGG CCAGGCAGTC TTGAACTCCT GACCTCAAGT 780 GATCCACCCA CCTCAGCCTC CCAAAGTGCT GGGATTACAG GCGTGAGCCA CTGTGCCCGG 840 CTCTGACTGG GCTATTTTCT ATCTTGATGG GTTTGCAACC TTGTGCCACA AAACAATTGA 900 AACCATGGTA TGTGTTGCTT AATGCATGTT ACTGATTTTT TGGACTTTTC ACAGCTCTGT 960 TACCTATCAT GCTTTTCTTT TCTTCTGTTT CTTTTCCTTT TCCTTTCTCC CCTCCCCTCC 1020 CCTCCCCTCT CCTTTCCGAG ATAGGATCTC ACTCTGTTGC CCATGCTGGA GTGCAGTGCT 1080 GTGATCATGG CTCACTACAG CCTTGAACTC ATGGGCTCAA GCAATCCTCC CACCTCACCT 1140 GATAGCTGGG ACCACAAGCA TGTACCATTA TGCCCAGCTA ATTTTTTTTT TTTGTTTTTT 1200 TGGTGGTAGA AATAGGGTGT CACTATGTTC CTCAGGCTGG TCTCAAACTG CTGGGCTTGA 1260 GCAGACCTCC CTCCTCGGCC TCCCAGTGTT AGGATTATGA GCATGAGCCA GCATGCCTGG 1320 CCTCTGCCAC ATTTTTTTTT TTTCTTTTTC TTTTTTTTAT TTTTAGTAGA AACGAGGTTT 1380 TGCCATGTTG GCCAGGCTGG TCTTGAAGTC CCAACCTCAA 1420
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