Tag | Content |
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EnhancerAtlas ID | HS048-14275 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr16:49590560-49591990 |
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) |
RREB1 | MA0073.1 | chr16:49591559-49591579 | GGTGATGGGGCGGTTTGGGT | - | 6.03 | ZNF263 | MA0528.1 | chr16:49591238-49591259 | GCCCCTGCCCGCTCCTCCTCC | - | 6.19 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_30375 | chr16:49590008-49592138 | Fetal_Muscle | SE_33405 | chr16:49587624-49601191 | H2171 | SE_66893 | chr16:49587624-49601191 | H2171 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I049556 | chr16 | 49590071 | 49591984 |
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Enhancer Sequence | AATTTAGCCA CCTGCAGTTA CTTCTTTATC CACAAGAGAG CACAGTGTCT TGAAGCTCAG 60 CACAAATTCT TTTGTAAATG CCTCGTGTAC TTATAGAACA CTGTATAACT CAAAAATTAT 120 AATTAAAATG TCTTAGCTCC TGTATTTATA GTAACATTTA AACTACTGTG CTTTCTTGAA 180 GTCAGTCATT TACTTGAGAA CAGCACACTT TACGGTGAAC AGATCTTTGA AACAGTACCA 240 CGGGGATCTA GCCCAGGCAC ATGTAACTCA ATATATGTCA ACAGCTGTAA AAATATTGGT 300 GGGAGAAGGC AGGAAAAAAA CTATGAGCCC AGATCAAGTG CCCTGTCTCT CATATCTGAC 360 TGTTTTCAGC TGCTCCCTCC TCTTCCAAAT AATTGGGCCA TTTTGGTGCC CGCTGTCACA 420 CAAGGCGGGC CCTCTTTGAG GCTGGATGAT CAAAAAGGTT ATAAATGAAA ATGATTTCGA 480 TGTTGGCGGC CTAGAGAGTG ACCAGGGCGT GCAGGGCGGC AGAGGGGCTG TTCTAATCTT 540 ACCAACTGCA CGCCGCCATC GGAGAGTATT CCTAGGGCGC GAGCAGCTCC CCAGGGTGAG 600 GCCACGGTAA ATTCTGCCTA ATCCCTTCTG CATACAAATG AGCGCCTGGC AGGAGGAGGG 660 AGGGGGGCAG ACGCCGCAGC CCCTGCCCGC TCCTCCTCCC CGGGTTGGCT GTCTTGGCTG 720 AACAAACAAG CCAGCGACAG TGGAGAGGGC TGCAGCCTGG GTGGAATGAG AAGGAGGAAC 780 TCCCGGGGCC ACCAGGGCTA GGGGAATTAC ATGAGGGGAT CCTAGGAGCA GGTGGCCCTG 840 GGGCAGTGTT CTGACCCTCT GACCCCAGGG GGTGGTGGTG GGGACACGGG TGCTTGGGTG 900 GAAAACGATG GCATGGCTGC AGGCCCCTGA TATTGGCCCA GGTGAGAGAA TGAAATGGCA 960 GCAGAAGCAG CCTCTGGGCT GGGGCTGGAG GAGCTGCCAG GTGATGGGGC GGTTTGGGTG 1020 GGAATCTGTC CTTCTGAAGG CACAGCACTG AGTTCACAAA GATGCAGAAA CTCATCTCCC 1080 ATGAAGGCCT CAAGGATGGT AGAAGGCCTC CTCCCACCCA CAGGATGAGC ACGCAGGAGG 1140 CCCAGGAAAG GCCAGGAGGA AGAGCCTCCA TCCTGAGCCC CCTTGGTTCC AGCCCTGCAA 1200 GGAAGTGATC AATTCAATTC TGGCAGCCAG ATCTAGAGAA GGAGTCTGGG CCTGGGCACC 1260 TGGGGCCCCC AAAGCCAGAG AGGGCTGGCT CCAGAGGGGC TGAGCCTCAA ACAGGGAAAC 1320 AGCCCACAGA GGGGAAAAGA CGAGGGTCCC ACCACAGAGA GAGCCAACAG ACAGCCGGAC 1380 TGGAGCTACA CAGTGTCATC CTGCAGTGCT GGAGGTTTCT GAAGCCAGTT 1430
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