Tag | Content |
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EnhancerAtlas ID | HS122-00085 |
Organism | Homo sapiens |
Tissue/cell | LoVo |
Coordinate | chr1:16289590-16292460 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DMRT3 | MA0610.1 | chr1:16289852-16289863 | AATGTATCAAA | + | 6.02 | IRF1 | MA0050.2 | chr1:16290668-16290689 | AAAGTGGAAGAGAAAGTGATA | - | 6.77 | IRF1 | MA0050.2 | chr1:16291221-16291242 | AAAATGAAAATGGAAGAGCAA | - | 6 | KLF4 | MA0039.3 | chr1:16290468-16290479 | GCAGGGTGTGG | - | 6.62 | Lhx3 | MA0135.1 | chr1:16289603-16289616 | AAATTAATTAATT | + | 6.92 | Lhx3 | MA0135.1 | chr1:16289604-16289617 | AATTAATTAATTT | - | 6.92 | MEF2C | MA0497.1 | chr1:16291053-16291068 | AAGACAAAAATAGCT | + | 6.05 | Nr2f6(var.2) | MA0728.1 | chr1:16291392-16291407 | GAGGTCAGGAGTTCA | + | 6.22 | POU6F1 | MA0628.1 | chr1:16289605-16289615 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr1:16289605-16289615 | ATTAATTAAT | - | 6.02 |
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| Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
SE_01097 | chr1:16287965-16290134 | Adrenal_Gland | SE_02709 | chr1:16291780-16293317 | Astrocytes | SE_03452 | chr1:16289829-16290282 | Brain_Angular_Gyrus | SE_03452 | chr1:16291596-16293383 | Brain_Angular_Gyrus | SE_04408 | chr1:16289595-16293617 | Brain_Anterior_Caudate | SE_05249 | chr1:16287827-16297050 | Brain_Cingulate_Gyrus | SE_06124 | chr1:16286945-16296922 | Brain_Hippocampus_Middle | SE_07342 | chr1:16287975-16297074 | Brain_Hippocampus_Middle_150 | SE_08131 | chr1:16288406-16296945 | Brain_Inferior_Temporal_Lobe | SE_18522 | chr1:16289418-16295180 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19255 | chr1:16289594-16294260 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_38820 | chr1:16291637-16293540 | HUVEC | SE_45001 | chr1:16292008-16293377 | NHLF | SE_45986 | chr1:16291429-16293624 | Osteoblasts | SE_55849 | chr1:16288535-16295464 | u87 | SE_61132 | chr1:16274043-16303645 | HBL1 | SE_67570 | chr1:16288535-16295464 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 16291784 | 16292062 | chr1 | 16291891 | 16292149 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I015961 | chr1 | 16288199 | 16293984 |
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Enhancer Sequence | CTAAAGAATA TATAAATTAA TTAATTTTAA AAGACTCACA CAATCCAGAA GTGAACATTA 60 CTAAGCATTA ATATATTCAC AGTTTGCTGC TGCCAGATGA ACTGCAAAAT GAAAACTATG 120 AAACAACTCC ATTTCTGGCA AAGGTGCCCT GGCCAATTCT CCCACCGCAA ACAGCCACAA 180 ATGCTGACTA AAAATGATAA GACATCTTTT AAAATGCATT AAAGATTGGG AATGATAGTA 240 AGAGGAGTTA AAAATAAAAT AAAATGTATC AAAGAACTGA TAGGTCAGTA AGTAATACTG 300 AGAGGTCAAA ACACATCTAA ACAAGGGTTG AAATCCAGAG AGCAAGTGGA GCTTTGAAAC 360 CAGGTTTCAA GAAAAGACAT TTGCAGAACT GGGCAAGCTT GAGCCCCACC CTCCACCCCA 420 TCCCCAGAGG GAGGTCTCAC TGAACCTTGG TGGAAAGAAG ACAATACAGA AACTGCCTAT 480 ATCAAATCTT GGTGCTGAAC AGAGGAGGGA AAAATCTTCC CTGAGAATGT ATAATGATTA 540 GCAGTCCCCC AAAAGGACTA CAGCCCAAAT TTACACCTTA TGAAACACAT ATTTCAGGCA 600 GATGAAAGTG ATCCCAGAAA GAAAAGTATT AAATGCAAGA AGGAAGGAAG AACAATGAAA 660 GTAGTATATA TATAAGTGAG CAAACCTAAA CAAATGCTGA ACTAATGATG CTCATAAAAG 720 TTGTAAAAGG ACTGGCACAG TGGCTCACAC CTCTAATCCT AGCACTTTGG GAGGCCAAAG 780 CAGGAGGAGT GCTTGAGCCC AGGAGTTCAA GACCAGCCTG TCTTTACCAA AAGAGACCCT 840 GTCTTTACCA AAAAAAAAAA AGTAAAAAGT AAAAATTAGC AGGGTGTGGT GGCGAGTGCC 900 TGTGATCCCA GCTACTCGAG AAGCTGAGGC AGGAGGATTG CATAATCCTA GAAGGTCCAG 960 GCTGCAGTAA GCTGCGATTG TGCCACGGCA CTCCAGCCTG GACAACAGCG AGACCCTGTC 1020 TCTAGAGAGA AAAAAAAAAA AAGGTTTAAA AAGAACTAAA ATGCACACCC ACAGAATAAA 1080 AGTGGAAGAG AAAGTGATAG CAATTAAAGT GTTCTCAGGT CCTCACTGTT TGAGAGTAAG 1140 GTATAAAGAC ACTGACTAAA TTTAGACTTT GATAAGTTAT GTAAATTGAA AGCTATACCA 1200 CATTTATGGA TCAGATGACT CAACATCATA AAAATGTCAG CTCTACCCAA ATTTATATAT 1260 TATAAACTCA ATGCAAATTC TAATAAAACA TACCAACAAT TTTTATGGCA TTTGACAAAT 1320 GTAATCTAAC ATGACAATGG GGCCAGGCAA GATGGCTCAC GCCTGTAATC CCAACACGTT 1380 GGGAGGCTGA GGTGGGAGGA TTGCTTGAGC CCAGGAATTC AAGACTAGCT TGGGCTACAT 1440 GGTGAAACCC TGTCTCTACA AAAAAGACAA AAATAGCTGA GCGTGGTGGC GTGTGCCTCT 1500 AGTCTCAGCT ACTTGGGAGG CTGAGGCGGA AGGATAGCTT AAGCCTGGGA GGTCAAGGCT 1560 GTAGTGAGCC AAGATCACAC CACTGCACTA CAGCCTGGGT GACAGAGCGA GACCCTGTCT 1620 CAGAAAAAAA TAAAATGAAA ATGGAAGAGC AATGGGCCAA GGATTTACTA GACACCAGTT 1680 CACCAGTTTT CTAAAATGAT GTATTTTACA AGTCAGTGTG GTATTTAAAC AGAGAACAGG 1740 CCGGGCACGG TGGCTCACGC CTATAATCCC AGCACTTTGG GAGGCCGAGA TGGGTGGATC 1800 ATGAGGTCAG GAGTTCAAGA CCAGCCTGGC CAAGATGCTG AAACCCCGTC TACTAAAAAT 1860 AAAAAAAAAT TAGCCAGGCG TGGTGGCACG CATCTGTAAT CCCAGCTACT CAGGAGGCTG 1920 AGGCAGGAGA ATCGCTTGAA CCTGGGAGGC GGAGTTTGCA GTGAGCTGAG ATCGCGCCAC 1980 TGCACTCCAG CCGGGGCAAC AGAGTGAGAC TCCGTATCAA AAAAAAAAAA AAAAGAATTT 2040 CTGCTCATCA AAAACAAAAA ACAATATCCT ACAGTGAAAA GACAAGCCAC AAACTGGAAG 2100 TAGGTAGTTA TAACACATAT AACTGACAAA GAATTAGTAT CCAAAATAAG AAATAAAAAA 2160 CAAAAAACTA ACAAAATGTC TACAAACCAC CCAATAGAAA AATGAGCAAG ACAATCTGTT 2220 GTTTCCGAGA AGATGAAATC TGAATGATCA GTAAGCAACG AAAAGATGCC CAACTCAGAA 2280 CCAGGAAAAT GCAAATCAAA ACCACATGAG ATGTCATTGT ACGCCCACCA GATTAGTAAA 2340 AATGTTGAAG TCTGAAAATA CCATTGTTGA GAGGATATGA GGCAAACGGA ATTGTTGAAG 2400 GGTAAACTGG GGAAACAGTT TTGGCAACAA CTTGGCATTA TTTGTTAAGT TGAAGACGCA 2460 CATACCCTGT GACTCCACTC CCAGCTGCAG TCCCTGGAGA GGCTGTGCAT ACATGTCCCG 2520 GGAATGTGAA CAGTGGCACT GTTTGTCTCA GCAAAATACT GGAAACAACC CAAATGTCCA 2580 CCAGTAATAG AAAGGATAAA TAAATTCTCA TACAATGGAA CATTATTCAT CTGTGAAAAT 2640 GAAATACCAC TCTATGCAAC GTGGATTAAT GTCAAGGCAC TGAAGAAAAC AATATGATTA 2700 TATTAAGTTC AAAAACCTGC AGAATTAAAC GGTACATTGT TTAGCAATAC AAACACATGG 2760 TAAAACTATA AAGAAAAGCA AGAGTGATAA AAGCAAAACT CAGGGATGAC TTGGGCCGGG 2820 TGAGATCAGG GAGGGGACAC AGGGGACTCC AAAGGTAACA GTAAGTTCTT 2870
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