Tag | Content |
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EnhancerAtlas ID | HS007-07157 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr17:49030780-49033770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr17:49031054-49031075 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 | IRF1 | MA0050.2 | chr17:49033556-49033577 | TTTTACTTTTTCTTTTTCTTT | + | 6.89 | 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: 21 | 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 | chr17:49030927-49033111 | 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 | CCTGTAATCC CAGCACTTTG GGAATCTGAG ATAGGAGGAT CACTTGAGCT CAGGAGTTCG 60 AGACCAGCCT GGGCAACATG GCGAAACACT GATTCTGCAA AAAATAAAAA AAAAATTAGC 120 TGGGTGTGGT GGTGTGTGCC TGTAGTCCCA GCTGCCCGGA GGGCTGATGT AGGTGGATAG 180 CTCCAGCCTG GGAGGTTGAG GCTGCAGTGA ACTATGATTG TGTCACTGCA CTCCAGCCTG 240 GGCGACAGAG GGGAGACCCT GTCCCAAGAA ACAAAAAAAA AAAAAGAAAG AAAGAAAGAA 300 AGAAAGAAAA AGTGGGCTCT GGAAGGAGCC AGCCACCGTT GCCCTCTGGG CACTCACCAT 360 CTCACCCCTC AGGCTCCAAC AGGGTTCCAC GTGACCAATC CCCGAGGGGA GAGGAGACTG 420 CGGAGAGGAT GGGAGGCAAA GCACCTCCTT CAAGCTCCAG GGAGGCAGGA GGATTTGTTT 480 AGGAGTGGCC CTGTGCAGAG GTAGGGGCAT GGCTGAGAAC ACCTTGGGAG GTGGTGTGAA 540 GCTGAGTCCA GGAGCCGCCA GCCCTCCCTG CCACTCAGCT CAGGGGTCAC TTGGGTAGCT 600 TCAGCCTCAA CAGCCGTGGA GTCAAGTGTC TCCTCTACAA AAATAATTCC CAAATAAGTC 660 ACTGCCTTCA CCCCTGGGAC TGGCTGGTGC ACCCAAATTG GAGTCGCCAC CCAGCCCCCT 720 TGAGCATTGC CTTGCTGGCT GATCCAACAG AGGCAGAATT AGCTGATGAG GCTACCACAG 780 CGGGAGGGAA CTGACCTGAG GCCGCCTGGA GAGATGGGAC CCCGAGGGCC CTTTCTGGCA 840 CTACTCACTT GTTGGGTCTG GGGAATTAAA ACACACTCCC CCTCTCTGGG TCTCAGTTTA 900 ACAGGGAGGA GACCACCACC TTCCAAACCT CAGTGACGGC ATCAGGCTGG GGGTGGTGCT 960 GGGCCTCCTG CGTCTGTGTC TGGAGACGCA GCTGACTCCC TGACAAGCCC AGACATGCAG 1020 CTGTTCCTGC AGAGGAAGCA GCAGGAACTG GGGAAGGGCA GAGCGCTGAG GGAGGGGCAA 1080 GAGGGATGCA AGGACACCAC AGTGACCGCG TGCAGCGAAG CGAGTATGAG CAGAGTCCCA 1140 ATCTCCAGGT CCCCTCTCCG CGGAAGCACT TTTGTCTTTA TTGGAAATTT CCTCCCATGT 1200 AACATCTGAC CTCTACCTTC TCTTCTACAG ATGAGCTCTG CTGTGAGTCC CAGCGGGCTG 1260 AGACACTGTG ACTGCCCACC TGTCCCCAGG TGCCCCTTCT ATACAGCCCC ATCCCTTCCC 1320 AGGGATGCTC AGTGGCTGCG GCCACCCTTG CTTTCTGCCA CTCAGCCCTT GCAGGGGCTT 1380 CACACCCCAA GAGGGGCAGT CTGGGCTGGG GCTCCTGGAC TCCCTAAGGC ATTATCCCAT 1440 CCCCGCAAGT TGCCCGGCCG GGCCCTGAAG GAAAGGGGCC CCGGACCCAG ACCCGAAGGC 1500 TGCTCACCAG AGGCTCTGCC CAGGGACTCT CACCTCTCCA GCCACTCCAA CTCCCCTCCG 1560 GCTTTCCTGT CATTTCCTGA TGCCACAAAT CTTCTGACAT CCTCCCTCTT CCCCAGTGAA 1620 TTTCTTCCCC AGGCCCTTCC CTTCCTCAAC CTGCTTCATA CTGGACATTC CCAGCTGGTA 1680 GGATCTGCCT GTGGCTCTGC ACAGGAGGCT GGGCAAGGGT GGAGAAGACT GGGGGAGCTG 1740 TCTCCCATGA CCCCAGCAGA GGCGAGAGAC AGAAGCTGCA TCTGGGACCT GTCGGCTGCA 1800 GTTTTGGGCA TTCATACCCA CCTAAGCATT CTGGAACAGC CCTGAACCTG GGCATCAAAC 1860 TCCCCAGGCT TGAGAATGGT GAACACTACT ATTAGGCGCC CCTTCCTCCA GGCCTATGCC 1920 GACTCCCCTG TGCCCATGGA AGCTGTGTAG TCCATGCTGG CTCTGGCTCA TGTGGGTGTC 1980 CGGACAGTGA GGCCGAGGCG GCAAGGGCCC TTTACTCTGT GCACTCCCAG CTCCCCATCC 2040 CAGCCAGGGC AGCCTTGACC CTCCTGCCCC CTTGCTGTGC CATGTGTCAG TTGGCTGGGA 2100 TCATGCTCTT CCCCCGTCTC CATCAAGAGG ATCCAACAGC ATCTTGCAGC TAACACTGGG 2160 GCATGGGAGT GAGGGAAACA AACATGGTAC CCACTCTTCT GTCCTAATGT TTAGAATCAT 2220 GGGGCAGAAA AGCATCCTAG AACTCATCTA GCCCAACTGT CATTTTACAG AAAACAGGAC 2280 AGAGAGAAAA TGACCAGCCT AAAGCTCTTG GCTACTCAGG GCAGCTGGGA CAGGGGTCTG 2340 GTTTCCCGGC ATGGAGCCAC AGTGTCTGGA TGTGCTGGAA CTCGGCACGT CCCCCTGAGA 2400 GTTAGCTGCA GAGGTGGCGT ATGGGAGAGG AGGCTGGAAA ATAGGCTTGG AGGTTTCGTC 2460 CAGGCACACA GATTCTCTCC CCCTAATCCT CAGCCCCTCC TTTTCTCCCT TTCAGCAGCA 2520 GTTATAAAAT CCAGGAAATA AATGTGGATT GATGGCCTAC AAAGGGCTTA GTTAGTGCTG 2580 TGACCTGCTG AGTTATGTAA CTGCTATTTA TTATCGGCCT TGGATGAAGT TTCCATTGAA 2640 GCAACTCACT AAGCTGATTC CGTGACATTT CTTTTAGCCT TGTTCAGAAG CAGCAGCCGC 2700 AGAAATTCTT CTGAAACTTC AAAGACTAGA AATTGATAGC GTGGATGCTT TTAAAGATTC 2760 CCTTCTTTCA TCCTTTTTTT ACTTTTTCTT TTTCTTTTTT CTTTTGAGAT GGAGTCTCGC 2820 TCTGTCACCC AGGCTGGAGT GTGGTGGTGT GATCTCGGCT CACTGCAACC TCTGCCTTCC 2880 AGGTTCAAGT GATCCTCCTG CCTCAACCTC CCAGAATAGC TGGAATTACA GGTGTGCACC 2940 ACCACACCCG GCTAATTTTT GTATTTTTAG TAGAGACGGG GTTTCACCAT 2990
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