Tag | Content |
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EnhancerAtlas ID | HS050-02332 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:53976560-53979390 |
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 | AGGGGGATGC AGGCTCTAGA CTGTGCACTC TGGAAACTCA TGTTCTGAAA CAAGACTGCA 60 GTGGCTGAGA GCAGCACAGG TGCCCTGAGC CCAGCCCAGC CCGAGGGCCC ACTACCTGGA 120 CCACAGGATG CTGCAGGCCA GGTTCCCTTC TCATGCTACC TTCCTAAGCC CCTGGGCCCC 180 GTTCACAGGG GCTAAAATGA CTTTGGGATC AATGGCTTGG GGGCTCTGGG GACAAGGCTG 240 AAGGCTCCCA GCCTGTAAAG CATTTATGTA CATGGCAGAA AGAGGGAGAT AGTGAGAGCT 300 CGGAGTCCCC ATTTTCTTGT CTGGATTTGT GGCTTGTTGG ACCATCCACA TTAAAATATA 360 CAGCGAATTC AATGTCACAG CTCCAGGTGA CCTCGTGACC CTTGCCCACC CTCTGAGACA 420 CCAAGTATTG ACAAACAGAT CAGTGCCTCT CTGAAGGAAG CAGGGCTATC TGGAAATGGG 480 GAAAGCAGAT TTGGAGAGAG GCTGGGGTCT CCGCATCTGT GCTGTGCCAA GTTCCTCTCT 540 GCTCCCTCCA ACGTTGGCAG CCCCTCCACT GCCCCTCCAG TCTGCTGTCA TCATCCACAC 600 GTGTGGGGCC CCCGTCACTG TGAGCTCGCT GAGGACAGGG GAAGCAGGGC CTCGGTGCTG 660 GGTCCCTGGC CCGGCCACTG ATACACTGTG GGTCCCTGTC ACTGTTTTAA GTTCATGAGA 720 CGAATCCTCA TCACACCTCC AGGAATAAAT TATCATTATC ATCATCATTA TTTTTAGGCC 780 TGTCTTGTGG GGTGATCAAG TGGGACAGCG TCTTCCTCTA TGCACTAGAA ACCGTGGACA 840 GCTGTGCACG AGCTGTGTGT TCTCATGACC AGTTCTGGCT GAAGCTGGGC TGGGGCCTGG 900 CCGGAGAGTG GCTCCTCCTT CCTGCAGGCC TGCTGTGTGG TGGCTGCCTT ATCCCCATCC 960 CATCTGGGCA CCCACAACCC AGCCCTCCCC TGGTTTCCTG AAGCCCCTGT AGGGAGGGCC 1020 AGGTCTTGGC CCTTCTCGGT CACCCGGTGC CCAGCGCTGG GCATGGCACA CAGTGAAAAA 1080 CCAATGACAC TAATAAATGA GTTTCTGAAT CTCTCAGTTG CAAATCCCAG AGATTAACAG 1140 CATTGCAGGA TTAAGATGAA CCAGATATGA AGGGGAAAAA ACATGTGTTT TCAAAAGTTT 1200 GTTTTTCCTG TCTCACTCCA CCATAAATTC ACATTTGCCA CCTTCACAGC TGGTGAAATT 1260 AAACAGAACA CAACTCTCTC CACAGCAGAC ATGACGCCTG AGGCTATGCT GCTCTACCTG 1320 AACCCTTTAA AAGGCAAAAA AGATCTTCTG GAGCTCCTCC TCTGAGTCAT GCAAATGATT 1380 CCTAAATCAA ATATTTTTGC TTCAACTGGA ACCTATAAAA ATTAATATAA AACCTCACTA 1440 GCCTGGCAGA CTGAGGGCTT CATACCTCGC ACAAGGCTGG GAAAAAAAAT ACCCTATTCG 1500 GCGTCTTCTC TGAGCCAGGG TAAATAAATT TGGTCATGAA GTCAGGCCCT CTTAGCATAT 1560 TTTTGAGTGA ATCAGATAAT TCTGTCAAGC TATTTAAACG TCCCAGCAAA CCACTGGGGA 1620 GCCACGAGTG GCCGTTCCTT GTTGACTTTG GCAGGAAGTG GAGGCTGAAG GCCCTTTCCC 1680 CACTCTCTTC TCAGGGGATG AAAAAAGAAA CCCATTCACG CTGGGCCTGG GCCTGGTGTC 1740 AGGCACGAGG ACGCTTCTCT CCTGCAGCTG GACCCGAGGC TCCTACCCGC AGGCAGGGGT 1800 GGGCAGGCGG GGGTCCCGTC TTGTCATCAC TCTGCTTCTC ACTGCAGAAT TCTTGACGGG 1860 CACTTATGCA GGCGGCAGGC AGGTGATGAA TGAGGCGGAG CAGAGTGCAC GGGCCCAAGC 1920 AGCGAACGGC CTTCGTGGTT TATTTTCCTT TGGTTGGAGA TGTTTTTCGG CTGGTTGGTG 1980 GGTGAGCAGG TGGCCTGAGC AGCTATGGGT GGGGGCGGGG ACCATCGTAG TAGAGCCTGT 2040 GCCAGGTGAG GCACACAGTG TCAGGCGTGT GTACGGCCCT CACCACCTTC CTCAGGGAGG 2100 GCCTTATAAT GCCTTTCACA GAAGCAGCAG CTGAGGCTCA AGGAGGGCCC GGTTTTCTGG 2160 GTCCCCCTTT GCACCCCCTT CAGGCTGCCT CTTCATGGTT CTCTGCTCAC ACTCACAGCC 2220 ACAATCTTCC CCTGCCTGTC AGCAGCCCCT CTGGACCCCC AGCTCATCCC TGAGGCCTCC 2280 TCCTCTCCCT GCCCAGCTCG GATTTCCTAC TCCCGCTGCC TCCAGTGCCA CCACTGCCTT 2340 CCGGGCTCCC CCTCCCCAGC CTGAACCAGG CCCTGGCTTG GGATGCTGTC TGTCCAGCGC 2400 CCCACAGTCC ACCCCACCCC TGCAATGCCG CCCTGCGTCC TCATCCCCAA ACCTGACCAC 2460 ATCACTGCTC AACACTCTTC AGGTCGAGTC TCATCCCAGG CCTTGGGATC TGGACCTGGC 2520 GACATCGCTC CCAAGTTCGT CACCCCACAC AATGACTCAT GTTTCCCAGA ACACCCCAAG 2580 CTCTCACCAT GCCTACCTTC ACTCTTGCTA CTCCTTCCTC CCAGCTTCTC CACTCATCCA 2640 ACTCCAGCCT CACCTCCTCC AGGAAGCCTT CCCTGACACC CTCCTGGCAG CCACACCCCA 2700 CTGGGCTCTC CTCTGGGCTC CACAGCCCTT CTGCTTCCTT GCCGCACACC ACTGGCCCCC 2760 TGTGTGGTAG GTCTCCCTCT CACAGTAAGC ATCTCCAGGG CCAGAGTCAT CGAGGCACCA 2820 GCACTGGGCC 2830
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