Tag | Content |
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EnhancerAtlas ID | HS048-26062 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr3:111815980-111816970 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Esrra | MA0592.2 | chr3:111816794-111816805 | CTCAAGGTCAT | + | 6.02 | Esrrg | MA0643.1 | chr3:111816795-111816805 | TCAAGGTCAT | + | 6.02 | FOSL1 | MA0477.1 | chr3:111816461-111816472 | GGTGACTCATG | + | 6.62 | FOSL2 | MA0478.1 | chr3:111816460-111816471 | GGGTGACTCAT | + | 6.14 | JUNB | MA0490.1 | chr3:111816460-111816471 | GGGTGACTCAT | + | 6.32 | JUND | MA0491.1 | chr3:111816461-111816472 | GGTGACTCATG | + | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_28388 | chr3:111815231-111817170 | Fetal_Intestine | SE_29441 | chr3:111815600-111817165 | Fetal_Intestine_Large | SE_64937 | chr3:111815177-111817048 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I112095 | chr3 | 111814575 | 111817231 |
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Enhancer Sequence | AAAGCCTTCA TCTTTTTCTC AAAGTCATTT TCTTTCTGGA TAATTTGGAG GATCAGTTGA 60 GTGTTCTCAA GGGTTCTCCT TTCTTCAATA ATTCACCCTA GTCATGGAGA GGTGAGACCC 120 TGAATAACAC TTTACTAATG AAGTTTTGGT TGGGGCAAAA TATTTTAAAT ATTTCAAAAA 180 CAAAACTGTG ACAAGTAGGT GGATGCTTAG AAACATGATT TAAATTGATA ACATCCTGGA 240 GACCCTCATG TGATATCCCC CAACATTATA CCCCAGATTC TTGCCTGACC CTAATCTCTT 300 AATTTATACA CCTTTTATGA GTAGGAACGC TGTGGTACTG AGATATAAGC AACGACTTCC 360 TAAGTGACGT TGTGTTGAGT GGATTTGTTT GCCTTTCAGT TGTGAATAAG AGCTACATTT 420 TATGATGTCA TGTGGTTCTG GCAGACTGAC AGTTTTCACA GGGTAATGCT CCCTGGTGTA 480 GGGTGACTCA TGGGAAAATC CTAGGCAGAC AGCATTAACA AGCTATAAGC TGCCAAGGTC 540 CTTTGGGGCA GGAACATGAG AGCAGTGCTA GACCCAGTAC CTTGAAATTT CTTTCCATTT 600 TCACCTGTTT ATCTTTTCTT CAAATCGCTG ATGTTTCTCT ACCAAGATGG ACACCCTTAC 660 CTGTGGTCTC CATATAATAT CTTTCAGCTT CCTCTGACCC AGAGATCTTC AGATATCTCC 720 TCCTCTCTCT AAGCATCCTC AGGTTCTTCT TAATTTATGC CTAGTGTTCC ATTATTGGAA 780 TGCTAATCAT GTAGAAGTTA TTTATATCTT ACTGCTCAAG GTCATCACCA AAGTCTGAAT 840 GCAAAAATTC GAAAAGTTCA ACCTCAGGTA TAAATGGGTT AACTCTTCAA ATGCACTAGC 900 ATCCTCTCTC CTTCAAAGCA ATCTTCCATC AGGATTCTTG CTACTTCATT TAGATATGTG 960 TTTTTCTCTC CCTTCTTTCA CTGGCACACT 990
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