Tag | Content |
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EnhancerAtlas ID | HS048-26198 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr3:124596320-124598560 |
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) |
EWSR1-FLI1 | MA0149.1 | chr3:124597648-124597666 | AAAAGGAAGGAAGCAATG | + | 6.19 | EWSR1-FLI1 | MA0149.1 | chr3:124597652-124597670 | GGAAGGAAGCAATGAATA | + | 6.31 | MEF2C | MA0497.1 | chr3:124598469-124598484 | TTCTATTTTTAAAAC | - | 6.49 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_00134 | chr3:124593431-124599388 | Adipose_Nuclei | SE_01601 | chr3:124596257-124598531 | Aorta | SE_47296 | chr3:124594568-124605888 | Panc1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I124875 | chr3 | 124594325 | 124599621 |
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Enhancer Sequence | CTCAGGCTCG TTGTGGCATA TCCTTTTCTT TGATATATAA AATCATTTTC ATAAAATCAT 60 GAGATTATAG CACCTTGGGG CTAGGATTGT TTTAAGATGA GCTAGTCAAG TTGCCTCTTT 120 TTATAGATGA AAATGTAAGA TAATGAGAGT ATGTGACTTG AAACAAGGAG CCCTATCTAC 180 AAAAAAGAGG TCAGACGGGG TCCTGACCAG CAAGTGCCCA CATGGGATAC CTGCCTGGTG 240 GTCCCTCTGC CATCTTGGAT GTAGGGCTGG TGTGACCTGC TGAGCTCTAG GGTCCTCTGG 300 AGATCTGTAA CAGCCCCTTT ATCAGAAAGG AATTTGAGGT CAAAGGCCTC ACGTAGGACT 360 CTGATCAAAG CCACATAATT TTTTTTTTTA GACAGAGTCT TGCTTTGTTG CCCAAGCTGG 420 ACTGCAGGGG CATGATCTTG GCTCACTGCA ACCTTGCTTC CCAAGTTCAA GTGATTCTCC 480 TGCCTCAGCC TCCTGAATAG CTGAGATTAC AGGCATATGC CATCACGCCT GGCTAATTTT 540 TGTATTTTTA ATAGAGATAG GGTTTCAGCA TGTTGGACAG GCTGGTCTTC TGACTTCGAC 600 TCCTGACTTC AAGTGATCTG CCCACTTCAG CCTCCCAAAG TGCTGGGATT ATAGACGTGA 660 GCCACCGTAT CCAGCTTCAA AGCCACATAC ATTTGCAAAC AACACTTTAT AATTACCAGA 720 GCCTCATCAT GAGCTCTGGG AACTTGGGCT GGAGGTCCAG GGCTCAGGAC AATAAGAGCT 780 CCTCAATTCT GATGCAGATC AGACTGAGCT CTGGTCTTCT GGTCCACCAG CCTAAAAGCC 840 CTTACTTAAT TGGACACAAT ACCAAAGAAA CTCAAAGGAT GTGATAGTCA CCTGGTATGA 900 AAACATCATG AACAACTGTA AAACAATTTG TCATATAGCA TTACTAACTG TTTCTGTTAT 960 TATTAAATAT TCACATGGAA AAGTAAAGTC GTTTGTACTC AAAATGATTG CCCTAAAATT 1020 CAGTTGCTGT TGGGACACAT TCAAATTCAA GAAACTCTGC ACTTAACACA CCCTAAACGC 1080 TGAGCACTGG ACTGGGGGGA TGCTAGAAAT GCACAGGTGA ATGACCTACC AGCCCTTGAT 1140 GTCCAGGAAC TCACAGTGTG CCGGGTACCA GGTACCAGAC AGGTACTCCA GGATCCAAAA 1200 CCACAGGCTG TGTGCTGGTA TGTGTAATGT CAGACTCACT CCCTTTGGCA TCTCTCCTCT 1260 CTCCACCTAT TAATATTTCA GAGTTTGGAC TTTGCTGGAT GAGTCATTTG GCACCAATAA 1320 GCATTTTGAA AAGGAAGGAA GCAATGAATA AAAAACTAAA CACACGGAGT TCACAAATGT 1380 CAGTGTTAGG TCTAGGTCAT GGAAACAGGA ACTAGCAGCC CAGATGATAG CCACATCTCA 1440 TCTTCTTTGC TGTTTGCATA GTGACTATTC CCAGCTCGGT GGCAACTCCA TGTATCTCTT 1500 TTGCCTCACG TCTCTGAAGC CCAGTGTTTA CTGCAAACTG TAATCTAAAA ATATGTTCTT 1560 CCAAAATTCA CTGACTCACC CCTGTGTTTC ATCAATCATT CAAGGAGCCA CCGCATCCGG 1620 TTGATCACTC CTTTCAAGAT GCAAGAAATG TTTATCCTAA GCCAACCCTT CCTGTCTGCA 1680 ACCTCTAGCC CCAACAACCC AAGCCAGGCC CTCTGGTCTA AATTCCTGCC ATAGCCTCCT 1740 GGCTGGCCTC CTTCCATTCA GCCTCTCTCC ACTTCTGTAC ACCCCATGGG TCCAAGGTCA 1800 GACAACTACT ACTAAAACAT ACATCTGCAG TTGGAATTTC CTGATCCAAA ATATTCAGTA 1860 GGATAACAGA AGTGAATACA GAAGCTGAAA TGGCCTTTCT GCCTTGAAGA TGGCAATGCC 1920 CTGGAATGCT TCTCCCCACA CCCTGAACCA GGCCCTCACA TTTGTCACAC AATGGACAAA 1980 AGAGTCCCAG TATAGACTCC AGCAACTAAA TAGCCATATG TCTAAATGTT ACCATGAAAT 2040 GCAAATATGC CCTAGGAAGG TTCTATCCCA GCAGTTCTCA TTCAAGACTG CCTTTATGAA 2100 CATCAGACAT CTGCACAACA CTCAACAATA CCAGCCTTAC AGATCTGACT TCTATTTTTA 2160 AAACACCAAT TCATATAATG GAGTGCTAGA CAGCTATAAA GAAAGAATGA GCATGCTCTC 2220 TGTATTGACA GGAAGCTTAC 2240
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