Tag | Content |
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EnhancerAtlas ID | HS048-37767 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr9:112250520-112252200 |
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) |
BCL6 | MA0463.2 | chr9:112250758-112250774 | TTGCATTCTAGGAACC | + | 6.05 | MEF2C | MA0497.1 | chr9:112252116-112252131 | GTTATAAAAATAGCA | + | 6.47 | STAT3 | MA0144.2 | chr9:112250881-112250892 | CTTCCCAGAAA | - | 6.02 | ZNF263 | MA0528.1 | chr9:112251281-112251302 | GGTGCAGGAAGAAGAGGTGGA | + | 6.37 | Zfx | MA0146.2 | chr9:112251903-112251917 | GGGGCCTAGGCCTG | + | 7.47 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27950 | chr9:112250535-112252173 | Fetal_Intestine | SE_28797 | chr9:112249166-112252352 | Fetal_Intestine_Large |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I109488 | chr9 | 112250424 | 112252059 |
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Enhancer Sequence | ACAGGCACCC ACCAGCACTG TGTAATTTTT TGTATTTTTA GTAGAGGCGG GGTTTTGCCA 60 CGTTGGCCAG TCTGGTCTCG AACTCCTGAC CTCAGGTGAT CCACCCGCCT CTGCCTCCCA 120 AAGTGCTAGG ATTACAGGCA TGAGCCACCG CACCAGGCTG AAAGTACATT TTTAAGCAGT 180 AAAATCTAAT AACACAGTTA ACCAGAAAAT CTTTCCAACA TTCAGCAGTA CTAGTATCTT 240 GCATTCTAGG AACCGGAACA TTCCTTTACT AACTGGCTTT TCCATTAAAG CTGCTGATGC 300 CTAGAGTAAT AAAAACACGA CTGCACTGGA CAGTGTTCTT AAAGTTCACA TGACTGGGAT 360 GCTTCCCAGA AAATAGCTCC ATTATCTTCA CATTTTCATC CTATAATAAT TTGTAATCCA 420 GGAAGGCAAG GTTTGTATTT TCTTCTAGGC AGAAAATAAG TTAAAGAACC AGACTGTATG 480 GATCCCAGAG CCTGACCCCT TGACCGAGTG TCTGGTCACT TGATATTACA AATCTAGACT 540 TCCTGATAAA TGGCCCTGTA GTGACCTTGT TACTGGGATC CCTAGATGCT GGTTTCCTGC 600 CTGGTTTCTC TGCATCCAAG TCCCTGTCTG CATCTACTGT CCATCCAATG CCCATCCTCT 660 TCTGCCTGGG TCCCCAATGC CACCTGCTTC CCTGCCTTTG CCAAAGGTCA GTGACTTAGT 720 CATCATCTCA GAACTAGGGC TGGAACAGGG ATGTGGGCGT TGGTGCAGGA AGAAGAGGTG 780 GAAGTGTGAG CACTAGAGGA AAGAAGATAA GGTCTAGGGT GACTCCCGCC TCCTGCCCTT 840 CTTTGCTTAC ACACCCTGGC TCTTAAATTC TATTAGAAAT TGGTCAGTGG GAAGCACAGC 900 TGGCTTGTTC ATCTCCCTGT CCATCTATCA TAAACTCTGT CCCTGCTCCT CCATCCAGCC 960 AGGGTATGTG AGTGACGTTC CAGACTCTGC CAGTCCTTGT GGCAGACAGG TACCATAGTG 1020 AGGTGAGAGC TGACAAAAGG CCGGTGTGGC AGGCACAAAG CTGGGAGTGG CATCCTACTG 1080 GAGGTGGGAC CACAGAGGTG TGGGGACCAA AGCCACAAAC ATCAGGCCTG CAGGCCATGC 1140 AGAGGTTAGT TTTGTCTTTA TCCAGGTAGA AGATTCCTAG TGCTAGAGGG TTTTCCATGC 1200 TGGCTCACCC TGCACTGATC TCAACCTCGA AGTCACTCTT AAATCCGGAC GTGACCACAC 1260 GTCCGGATTT ACCTAGGGCA GTCCCGGCTT AGACCCGTCA GTCATGTGCA ATTATTAATA 1320 GGACCCCTTT TTATTCTCAA ATTGTTCTGG TTGGGATGAT AAATTCTAGT TGCACTGTTC 1380 TTGGGGGCCT AGGCCTGTGA AGTCAGTGCT GCAGTTAGAG AAGTCTACCC ATGATTAGCA 1440 GGGACGCCCA GCCTGATGAG TCTCACCCCT CATCAAACAT TCCATTTGCC TCTCCAGTAT 1500 CCCTGCCAAA CCATCATCTG GCTTCTGCTT GTATATCTGC AAGGACAGCA GGCTCACTAT 1560 CTTCTCAGGA AGCCTCTCTT TTTTGGGGAA AGCTTTGTTA TAAAAATAGC AGGATTCAAA 1620 CCTGTATACA GTATGACTGC AACTAAATAA CAACATCCAG GCCGGGTGGG GTGGCTCATG 1680
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