Tag | Content |
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EnhancerAtlas ID | HS007-00496 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr1:53976570-53978760 |
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 | chr1:53976947-53976962 | TGACCTCGTGACCCT | - | 6.36 | SREBF1 | MA0595.1 | chr1:53977346-53977356 | GTGGGGTGAT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_33491 | chr1:53977320-53979867 | H2171 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I053511 | chr1 | 53977561 | 53978453 |
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Enhancer Sequence | AGGCTCTAGA CTGTGCACTC TGGAAACTCA TGTTCTGAAA CAAGACTGCA GTGGCTGAGA 60 GCAGCACAGG TGCCCTGAGC CCAGCCCAGC CCGAGGGCCC ACTACCTGGA CCACAGGATG 120 CTGCAGGCCA GGTTCCCTTC TCATGCTACC TTCCTAAGCC CCTGGGCCCC GTTCACAGGG 180 GCTAAAATGA CTTTGGGATC AATGGCTTGG GGGCTCTGGG GACAAGGCTG AAGGCTCCCA 240 GCCTGTAAAG CATTTATGTA CATGGCAGAA AGAGGGAGAT AGTGAGAGCT CGGAGTCCCC 300 ATTTTCTTGT CTGGATTTGT GGCTTGTTGG ACCATCCACA TTAAAATATA CAGCGAATTC 360 AATGTCACAG CTCCAGGTGA CCTCGTGACC CTTGCCCACC CTCTGAGACA CCAAGTATTG 420 ACAAACAGAT CAGTGCCTCT CTGAAGGAAG CAGGGCTATC TGGAAATGGG GAAAGCAGAT 480 TTGGAGAGAG GCTGGGGTCT CCGCATCTGT GCTGTGCCAA GTTCCTCTCT GCTCCCTCCA 540 ACGTTGGCAG CCCCTCCACT GCCCCTCCAG TCTGCTGTCA TCATCCACAC GTGTGGGGCC 600 CCCGTCACTG TGAGCTCGCT GAGGACAGGG GAAGCAGGGC CTCGGTGCTG GGTCCCTGGC 660 CCGGCCACTG ATACACTGTG GGTCCCTGTC ACTGTTTTAA GTTCATGAGA CGAATCCTCA 720 TCACACCTCC AGGAATAAAT TATCATTATC ATCATCATTA TTTTTAGGCC TGTCTTGTGG 780 GGTGATCAAG TGGGACAGCG TCTTCCTCTA TGCACTAGAA ACCGTGGACA GCTGTGCACG 840 AGCTGTGTGT TCTCATGACC AGTTCTGGCT GAAGCTGGGC TGGGGCCTGG CCGGAGAGTG 900 GCTCCTCCTT CCTGCAGGCC TGCTGTGTGG TGGCTGCCTT ATCCCCATCC CATCTGGGCA 960 CCCACAACCC AGCCCTCCCC TGGTTTCCTG AAGCCCCTGT AGGGAGGGCC AGGTCTTGGC 1020 CCTTCTCGGT CACCCGGTGC CCAGCGCTGG GCATGGCACA CAGTGAAAAA CCAATGACAC 1080 TAATAAATGA GTTTCTGAAT CTCTCAGTTG CAAATCCCAG AGATTAACAG CATTGCAGGA 1140 TTAAGATGAA CCAGATATGA AGGGGAAAAA ACATGTGTTT TCAAAAGTTT GTTTTTCCTG 1200 TCTCACTCCA CCATAAATTC ACATTTGCCA CCTTCACAGC TGGTGAAATT AAACAGAACA 1260 CAACTCTCTC CACAGCAGAC ATGACGCCTG AGGCTATGCT GCTCTACCTG AACCCTTTAA 1320 AAGGCAAAAA AGATCTTCTG GAGCTCCTCC TCTGAGTCAT GCAAATGATT CCTAAATCAA 1380 ATATTTTTGC TTCAACTGGA ACCTATAAAA ATTAATATAA AACCTCACTA GCCTGGCAGA 1440 CTGAGGGCTT CATACCTCGC ACAAGGCTGG GAAAAAAAAT ACCCTATTCG GCGTCTTCTC 1500 TGAGCCAGGG TAAATAAATT TGGTCATGAA GTCAGGCCCT CTTAGCATAT TTTTGAGTGA 1560 ATCAGATAAT TCTGTCAAGC TATTTAAACG TCCCAGCAAA CCACTGGGGA GCCACGAGTG 1620 GCCGTTCCTT GTTGACTTTG GCAGGAAGTG GAGGCTGAAG GCCCTTTCCC CACTCTCTTC 1680 TCAGGGGATG AAAAAAGAAA CCCATTCACG CTGGGCCTGG GCCTGGTGTC AGGCACGAGG 1740 ACGCTTCTCT CCTGCAGCTG GACCCGAGGC TCCTACCCGC AGGCAGGGGT GGGCAGGCGG 1800 GGGTCCCGTC TTGTCATCAC TCTGCTTCTC ACTGCAGAAT TCTTGACGGG CACTTATGCA 1860 GGCGGCAGGC AGGTGATGAA TGAGGCGGAG CAGAGTGCAC GGGCCCAAGC AGCGAACGGC 1920 CTTCGTGGTT TATTTTCCTT TGGTTGGAGA TGTTTTTCGG CTGGTTGGTG GGTGAGCAGG 1980 TGGCCTGAGC AGCTATGGGT GGGGGCGGGG ACCATCGTAG TAGAGCCTGT GCCAGGTGAG 2040 GCACACAGTG TCAGGCGTGT GTACGGCCCT CACCACCTTC CTCAGGGAGG GCCTTATAAT 2100 GCCTTTCACA GAAGCAGCAG CTGAGGCTCA AGGAGGGCCC GGTTTTCTGG GTCCCCCTTT 2160 GCACCCCCTT CAGGCTGCCT CTTCATGGTT 2190
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