Tag | Content |
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EnhancerAtlas ID | HS082-15027 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr17:49030510-49033430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr17:49031054-49031075 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 | Myod1 | MA0499.1 | chr17:49031795-49031808 | TGCAGCTGTTCCT | + | 7.34 | TP53 | MA0106.3 | chr17:49031781-49031799 | GACAAGCCCAGACATGCA | + | 6.37 | TP53 | MA0106.3 | chr17:49031781-49031799 | GACAAGCCCAGACATGCA | - | 6.54 | Zfx | MA0146.2 | chr17:49032768-49032782 | GAGGCCGAGGCGGC | - | 6.02 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_00952 | chr17:49030867-49035094 | Adrenal_Gland | SE_02991 | chr17:49032474-49033379 | Bladder | SE_04178 | chr17:49031015-49032189 | Brain_Anterior_Caudate | SE_05235 | chr17:49030956-49032312 | Brain_Cingulate_Gyrus | SE_06067 | chr17:49030165-49035186 | Brain_Hippocampus_Middle | SE_23191 | chr17:49031126-49031896 | Colon_Crypt_1 | SE_23784 | chr17:49031665-49031984 | Colon_Crypt_2 | SE_26011 | chr17:49032143-49033783 | Duodenum_Smooth_Muscle | SE_26691 | chr17:49030919-49033447 | Esophagus | SE_29967 | chr17:49030933-49033704 | Fetal_Muscle | SE_37666 | chr17:49025326-49036503 | HSMMtube | SE_47468 | chr17:49031102-49031460 | Pancreas | SE_47468 | chr17:49032629-49033381 | Pancreas | SE_48151 | chr17:49023159-49034340 | Psoas_Muscle | SE_49193 | chr17:49032258-49033530 | Right_Atrium | SE_51156 | chr17:49018220-49035057 | Skeletal_Muscle | SE_54412 | chr17:49030869-49034362 | Spleen | SE_54634 | chr17:49031082-49034752 | Stomach_Smooth_Muscle | SE_57824 | chr17:49030111-49030829 | VACO_503 | SE_57824 | chr17:49030927-49033111 | VACO_503 | SE_59738 | chr17:48979175-49044314 | Ly4 | SE_65373 | chr17:49030870-49033427 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr17 | 49032200 | 49032260 | chr17 | 49031200 | 49032200 | chr17 | 49031092 | 49031200 |
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| Number: 2 | ID | Chromosome | Start | End |
GH17I050952 | chr17 | 49030112 | 49030829 | GH17I050953 | chr17 | 49030850 | 49033890 |
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Enhancer Sequence | GGGGATTAAG GCAGGCAATG GATGAGGAAC CCAGGACTGG GCCCAGCACA CACTCCACAG 60 TTGCATGGGA TTCTCCTCTC CTAAGGACTT TTTGGCCTGG GACATGGTAG CTAGCGGGCA 120 GAGGTGGAGT AGGCACATAT TTTGGCTTTC ACGAGAGAAC TTTCTGAAAT GATCTTGATG 180 CTCCTGTCCC ACCCAGCTCA TGGCACAGTT TCTCTAGAAC AATCCCATGC TCATTTATCA 240 ACAAGGAAAA CCCAGGCATG GTGGCTCACA CCTGTAATCC CAGCACTTTG GGAATCTGAG 300 ATAGGAGGAT CACTTGAGCT CAGGAGTTCG AGACCAGCCT GGGCAACATG GCGAAACACT 360 GATTCTGCAA AAAATAAAAA AAAAATTAGC TGGGTGTGGT GGTGTGTGCC TGTAGTCCCA 420 GCTGCCCGGA GGGCTGATGT AGGTGGATAG CTCCAGCCTG GGAGGTTGAG GCTGCAGTGA 480 ACTATGATTG TGTCACTGCA CTCCAGCCTG GGCGACAGAG GGGAGACCCT GTCCCAAGAA 540 ACAAAAAAAA AAAAAGAAAG AAAGAAAGAA AGAAAGAAAA AGTGGGCTCT GGAAGGAGCC 600 AGCCACCGTT GCCCTCTGGG CACTCACCAT CTCACCCCTC AGGCTCCAAC AGGGTTCCAC 660 GTGACCAATC CCCGAGGGGA GAGGAGACTG CGGAGAGGAT GGGAGGCAAA GCACCTCCTT 720 CAAGCTCCAG GGAGGCAGGA GGATTTGTTT AGGAGTGGCC CTGTGCAGAG GTAGGGGCAT 780 GGCTGAGAAC ACCTTGGGAG GTGGTGTGAA GCTGAGTCCA GGAGCCGCCA GCCCTCCCTG 840 CCACTCAGCT CAGGGGTCAC TTGGGTAGCT TCAGCCTCAA CAGCCGTGGA GTCAAGTGTC 900 TCCTCTACAA AAATAATTCC CAAATAAGTC ACTGCCTTCA CCCCTGGGAC TGGCTGGTGC 960 ACCCAAATTG GAGTCGCCAC CCAGCCCCCT TGAGCATTGC CTTGCTGGCT GATCCAACAG 1020 AGGCAGAATT AGCTGATGAG GCTACCACAG CGGGAGGGAA CTGACCTGAG GCCGCCTGGA 1080 GAGATGGGAC CCCGAGGGCC CTTTCTGGCA CTACTCACTT GTTGGGTCTG GGGAATTAAA 1140 ACACACTCCC CCTCTCTGGG TCTCAGTTTA ACAGGGAGGA GACCACCACC TTCCAAACCT 1200 CAGTGACGGC ATCAGGCTGG GGGTGGTGCT GGGCCTCCTG CGTCTGTGTC TGGAGACGCA 1260 GCTGACTCCC TGACAAGCCC AGACATGCAG CTGTTCCTGC AGAGGAAGCA GCAGGAACTG 1320 GGGAAGGGCA GAGCGCTGAG GGAGGGGCAA GAGGGATGCA AGGACACCAC AGTGACCGCG 1380 TGCAGCGAAG CGAGTATGAG CAGAGTCCCA ATCTCCAGGT CCCCTCTCCG CGGAAGCACT 1440 TTTGTCTTTA TTGGAAATTT CCTCCCATGT AACATCTGAC CTCTACCTTC TCTTCTACAG 1500 ATGAGCTCTG CTGTGAGTCC CAGCGGGCTG AGACACTGTG ACTGCCCACC TGTCCCCAGG 1560 TGCCCCTTCT ATACAGCCCC ATCCCTTCCC AGGGATGCTC AGTGGCTGCG GCCACCCTTG 1620 CTTTCTGCCA CTCAGCCCTT GCAGGGGCTT CACACCCCAA GAGGGGCAGT CTGGGCTGGG 1680 GCTCCTGGAC TCCCTAAGGC ATTATCCCAT CCCCGCAAGT TGCCCGGCCG GGCCCTGAAG 1740 GAAAGGGGCC CCGGACCCAG ACCCGAAGGC TGCTCACCAG AGGCTCTGCC CAGGGACTCT 1800 CACCTCTCCA GCCACTCCAA CTCCCCTCCG GCTTTCCTGT CATTTCCTGA TGCCACAAAT 1860 CTTCTGACAT CCTCCCTCTT CCCCAGTGAA TTTCTTCCCC AGGCCCTTCC CTTCCTCAAC 1920 CTGCTTCATA CTGGACATTC CCAGCTGGTA GGATCTGCCT GTGGCTCTGC ACAGGAGGCT 1980 GGGCAAGGGT GGAGAAGACT GGGGGAGCTG TCTCCCATGA CCCCAGCAGA GGCGAGAGAC 2040 AGAAGCTGCA TCTGGGACCT GTCGGCTGCA GTTTTGGGCA TTCATACCCA CCTAAGCATT 2100 CTGGAACAGC CCTGAACCTG GGCATCAAAC TCCCCAGGCT TGAGAATGGT GAACACTACT 2160 ATTAGGCGCC CCTTCCTCCA GGCCTATGCC GACTCCCCTG TGCCCATGGA AGCTGTGTAG 2220 TCCATGCTGG CTCTGGCTCA TGTGGGTGTC CGGACAGTGA GGCCGAGGCG GCAAGGGCCC 2280 TTTACTCTGT GCACTCCCAG CTCCCCATCC CAGCCAGGGC AGCCTTGACC CTCCTGCCCC 2340 CTTGCTGTGC CATGTGTCAG TTGGCTGGGA TCATGCTCTT CCCCCGTCTC CATCAAGAGG 2400 ATCCAACAGC ATCTTGCAGC TAACACTGGG GCATGGGAGT GAGGGAAACA AACATGGTAC 2460 CCACTCTTCT GTCCTAATGT TTAGAATCAT GGGGCAGAAA AGCATCCTAG AACTCATCTA 2520 GCCCAACTGT CATTTTACAG AAAACAGGAC AGAGAGAAAA TGACCAGCCT AAAGCTCTTG 2580 GCTACTCAGG GCAGCTGGGA CAGGGGTCTG GTTTCCCGGC ATGGAGCCAC AGTGTCTGGA 2640 TGTGCTGGAA CTCGGCACGT CCCCCTGAGA GTTAGCTGCA GAGGTGGCGT ATGGGAGAGG 2700 AGGCTGGAAA ATAGGCTTGG AGGTTTCGTC CAGGCACACA GATTCTCTCC CCCTAATCCT 2760 CAGCCCCTCC TTTTCTCCCT TTCAGCAGCA GTTATAAAAT CCAGGAAATA AATGTGGATT 2820 GATGGCCTAC AAAGGGCTTA GTTAGTGCTG TGACCTGCTG AGTTATGTAA CTGCTATTTA 2880 TTATCGGCCT TGGATGAAGT TTCCATTGAA GCAACTCACT 2920
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