Tag | Content |
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EnhancerAtlas ID | HS110-03006 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr20:31059660-31062400 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Hnf4a | MA0114.3 | chr20:31061433-31061449 | GATGAACTTTGACCCA | - | 6.65 | MYC | MA0147.3 | chr20:31061150-31061162 | GAGCACGTGGCT | - | 6.04 | Nr2f6 | MA0677.1 | chr20:31061435-31061449 | TGAACTTTGACCCA | - | 6.15 | Rxra | MA0512.2 | chr20:31061435-31061449 | TGAACTTTGACCCA | - | 6.64 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_01118 | chr20:31060843-31065873 | Adrenal_Gland | SE_03291 | chr20:31061284-31061926 | Brain_Angular_Gyrus | SE_04048 | chr20:31059689-31066170 | Brain_Anterior_Caudate | SE_04930 | chr20:31057146-31071030 | Brain_Cingulate_Gyrus | SE_05885 | chr20:31047540-31074914 | Brain_Hippocampus_Middle | SE_06864 | chr20:31057423-31066366 | Brain_Hippocampus_Middle_150 | SE_07969 | chr20:31057244-31071007 | Brain_Inferior_Temporal_Lobe | SE_17373 | chr20:31061422-31066203 | CD4p_CD25-_CD45RAp_Naive | SE_23164 | chr20:31059880-31071430 | Colon_Crypt_1 | SE_23809 | chr20:31059955-31066646 | Colon_Crypt_2 | SE_24726 | chr20:31059872-31072878 | Colon_Crypt_3 | SE_27760 | chr20:31059930-31074602 | Fetal_Intestine | SE_28710 | chr20:31060148-31074579 | Fetal_Intestine_Large | SE_30561 | chr20:31060598-31066404 | Fetal_Muscle | SE_31615 | chr20:31059935-31066550 | Gastric | SE_35617 | chr20:31059709-31065488 | HepG2 | SE_38064 | chr20:31050845-31066068 | HUVEC | SE_42465 | chr20:31050564-31066270 | Lung | SE_47565 | chr20:31061546-31064345 | Pancreas | SE_50168 | chr20:31059715-31074357 | Sigmoid_Colon | SE_52531 | chr20:31059835-31074536 | Small_Intestine | SE_53462 | chr20:31060363-31065967 | Spleen | SE_54992 | chr20:31061852-31066039 | Stomach_Smooth_Muscle | SE_65380 | chr20:31059900-31066072 | Pancreatic_islets | SE_69043 | chr20:31060619-31065482 | H9 |
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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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Enhancer Sequence | CCCTTCACCT TCTGCCATGT CTGTAAGCTT CCTGAGGCCT CACCAGAAGC CAAGCAGATG 60 CTAGTGCCAT GCCTGTACAG CCTGTGGAAC TGTGAACCAA ATAAACCTCT TTTCTTTATA 120 AATTACCCAG CCTCAGGTAT TCCTTTATAG CAACACCAAA CGGACCAACA CAGGTGTGTC 180 ATCAGCACAG CCTTGGGAGT CCCCACACTC CCGGCGAAAA GAAAAGGCCC AGGTACTCAG 240 ATGGGAAGGA TGTCCCCAGA AACAAACAAC CCAACTTATC CCCCATCAGA GGCGGAGCTC 300 CATCTGCTCT GCAATGGTGT GCTTGGGTAG GTCTCAGTAA ATGTTTGTTC GTTTGTTCAT 360 TCGGGGATAA CAGACATTCA GCAGGTACCG ACAATGGGCC ATGTTCGCAA CCGAGTCCCA 420 GGGGCAGGGC AGAGACCAAG ACTGACCTTA CAGCAGGCCT CAGACTTCCA CGAAGGACGG 480 AAGGCCAGAG CCCACACACC AAGCCCACCT GGGCATCAGT GGGGTTGGGG GGCTTCTGCA 540 ATGGAGACCC TCGGGCGGGG AGTGGAGCAC ACAGAGGGCT AAAGCGGGTG CCTCTGCTTG 600 GGCTGTCCCT GCCTAGTCCT GCGTCAATAA CAGGGGCCTG AGAGTGCTCT GATGGGAGCC 660 CCTTGACTCA CTCATGGGAG CTGGACCTCA CATTTCTGCA CCGTGAGCAC CTTCAAGAGG 720 GGCTGGTTGT ATGTCTCCAG GGGGGCCAGA AGATGGCCCA GGACTCTAGG CTGGAAACCC 780 ACTGCTCTGG ACAGACACCA ACAGGCCCAC AGGCCCAGAA GAGGCAGCAG AGGCCAGGCC 840 AGCTGCCTGG GCCTTCCCAA GGCCTGTGCC CTGCCCAGGG TCTCAGCCAG CCAGCGGGGT 900 GGCCCACAAC TCCATGAGTG TCTCGGAGGG GACAGTGAGG CCCACGGCCC TGTGGTCAAC 960 AGCATCCTCC CTGTCCCAGC TCTGGTGTCC ATCAGGAGGG GAAGGTGGTG TCTGACTACC 1020 CCAGGCTGAC CCCGCACTGG GCTCTTGGGG ACCTACAGAC CCCCCAGCCT CCCTGCATCT 1080 CTCAGCCTCA TCCTCATGGC CAGGCCAGCC AGCCTCTGGG CAGCAGGTGC TGAGGGAACC 1140 CCATGGACCC CACAGAAATG CCACTGTCAG CTACCTGATC CTGACAGCCC CCAAATCACC 1200 AGACCTCCCC AGGACGTGTC TCCAAGAGAG ATCACGCTCT CAAAGGGTGG TCATGAGGAA 1260 TAACAGCATG AGATCTGCTT GGGAATGAGT AGGGGGACCA TGGTCCCTTC AGCCCCACTG 1320 CTCTGGGTTT CTGAACAACT GTCCCAGACC CTTCTTGTGG GGGACCACAG CCTGTGGCCC 1380 CAGCTGGGCT CTGCAGGCAC CGCCCTCAGT GTTCCTTGGG CGTGGCCTCA ATCGGCTCAG 1440 TTGAGGCGGG AGGTCAGCTG CTGCGCTTGT CCCAGCCCCA GAGCCCCCCA GAGCACGTGG 1500 CTGCCCCCGC CGGTCCCCAC CCCCGTGGGA ACGCTGGAAG GCGGCACTGG CCTGGGAGGC 1560 TGGCAGCACG AGGGGGTCGC ACCGACCTCA CGAGGCATCA AGCACAAAAG CCTTTTCTTT 1620 GCCGGCAGCC ACGCACCCCA CTCCTCCTGC AGCCACTCCC TGTGCTCCCC AGCCCCTGGC 1680 CCAGACACCT CCAGCTGCCT CCAGACTGGG TCTCCTCCCA AACAAAGCCG GATTCAGGCC 1740 TTCGGGAGGC AGGCGCGCAG GTTCTGCCAT GGAGATGAAC TTTGACCCAA ACAGCAAGGC 1800 TCCTACCCCT TATTTACTCT TTAAGGCTGA CCCGTTTCAC AGAGTTCACA TTACACCCCT 1860 TTTTAATCCG CACCTCCCTC CCACATTCCA GGCCTCGACC TTCAACCCCT CCTAATTGCT 1920 GGCTCCGGCT CCTACACCCC AGTTCTTGGG CCCAGCTCAC TCATCCCTGC CCCCAACCAT 1980 CTCCTCCACG GAAACAAAGG CGATGCTGGG GTGCTGTGCT CACAGGGCCA CCTCACAACC 2040 CTGGCACACC AAGGTAGATG CCAGGGTCCC AGAGCCCAAC CACTTGGGGG AGTCCACGTG 2100 GAGGCCGGGG TGGATCTTTG GGGTCTGATT CCTGACCCTA ACTCTCCAAC CCCTGAGAAG 2160 GAAGCCTCTA TTCCAAGGGA GGCTGGAGTA GGCTGCCTGG CAGGCCCTGC GCGGAGGCGG 2220 TCAGGGCTAG GGAAGAATCC GGACAGCTCC CCAGCCAGCC GCATCGCATC CCAAGGGGCT 2280 AGGGTGAATG TGGGCAGCTG CACTGCCTGG TCACTCACCA GGTGACCTGG GCTATAGCCT 2340 CACATGTGGC TGCAGAAACA CAGCTTGTTT CCCTTGCTGG GCAGCGGAAC TGCTCTGGGT 2400 TAGGTACACT GTGAACCTTC CCAGGCCTGC CCCTGGTAAC TCTGAAACCC ACATTGCAGA 2460 AGCCCATGGC ATCCCGGCAA CCAGGCAGAC CCCCCGCCCC GCAGGCTGCC AGTCCTATGG 2520 GCTCTCTCCC TCATCTTTGG GAGGAAGGAG CCAGGAGCTG GGGCACTGGG GCCCATGGAG 2580 ATGCTGAGAA CACTGGGGGC AGTGCAAGCT TGGGCCTGAG CCACCCAAAG GCCTTGGCCC 2640 AGATTCCGCC ACCCTGGAGT GTGTCCACAC CTCTCACCTG AGGACAACTG GGAGCAGGGG 2700 GCCGGGCACA GCCCCTCCTC AACTGCCACC AAGGGGCACT 2740
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