Tag | Content |
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EnhancerAtlas ID | HS182-13767 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr20:31059880-31062400 |
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 | GAAAAGGCCC AGGTACTCAG ATGGGAAGGA TGTCCCCAGA AACAAACAAC CCAACTTATC 60 CCCCATCAGA GGCGGAGCTC CATCTGCTCT GCAATGGTGT GCTTGGGTAG GTCTCAGTAA 120 ATGTTTGTTC GTTTGTTCAT TCGGGGATAA CAGACATTCA GCAGGTACCG ACAATGGGCC 180 ATGTTCGCAA CCGAGTCCCA GGGGCAGGGC AGAGACCAAG ACTGACCTTA CAGCAGGCCT 240 CAGACTTCCA CGAAGGACGG AAGGCCAGAG CCCACACACC AAGCCCACCT GGGCATCAGT 300 GGGGTTGGGG GGCTTCTGCA ATGGAGACCC TCGGGCGGGG AGTGGAGCAC ACAGAGGGCT 360 AAAGCGGGTG CCTCTGCTTG GGCTGTCCCT GCCTAGTCCT GCGTCAATAA CAGGGGCCTG 420 AGAGTGCTCT GATGGGAGCC CCTTGACTCA CTCATGGGAG CTGGACCTCA CATTTCTGCA 480 CCGTGAGCAC CTTCAAGAGG GGCTGGTTGT ATGTCTCCAG GGGGGCCAGA AGATGGCCCA 540 GGACTCTAGG CTGGAAACCC ACTGCTCTGG ACAGACACCA ACAGGCCCAC AGGCCCAGAA 600 GAGGCAGCAG AGGCCAGGCC AGCTGCCTGG GCCTTCCCAA GGCCTGTGCC CTGCCCAGGG 660 TCTCAGCCAG CCAGCGGGGT GGCCCACAAC TCCATGAGTG TCTCGGAGGG GACAGTGAGG 720 CCCACGGCCC TGTGGTCAAC AGCATCCTCC CTGTCCCAGC TCTGGTGTCC ATCAGGAGGG 780 GAAGGTGGTG TCTGACTACC CCAGGCTGAC CCCGCACTGG GCTCTTGGGG ACCTACAGAC 840 CCCCCAGCCT CCCTGCATCT CTCAGCCTCA TCCTCATGGC CAGGCCAGCC AGCCTCTGGG 900 CAGCAGGTGC TGAGGGAACC CCATGGACCC CACAGAAATG CCACTGTCAG CTACCTGATC 960 CTGACAGCCC CCAAATCACC AGACCTCCCC AGGACGTGTC TCCAAGAGAG ATCACGCTCT 1020 CAAAGGGTGG TCATGAGGAA TAACAGCATG AGATCTGCTT GGGAATGAGT AGGGGGACCA 1080 TGGTCCCTTC AGCCCCACTG CTCTGGGTTT CTGAACAACT GTCCCAGACC CTTCTTGTGG 1140 GGGACCACAG CCTGTGGCCC CAGCTGGGCT CTGCAGGCAC CGCCCTCAGT GTTCCTTGGG 1200 CGTGGCCTCA ATCGGCTCAG TTGAGGCGGG AGGTCAGCTG CTGCGCTTGT CCCAGCCCCA 1260 GAGCCCCCCA GAGCACGTGG CTGCCCCCGC CGGTCCCCAC CCCCGTGGGA ACGCTGGAAG 1320 GCGGCACTGG CCTGGGAGGC TGGCAGCACG AGGGGGTCGC ACCGACCTCA CGAGGCATCA 1380 AGCACAAAAG CCTTTTCTTT GCCGGCAGCC ACGCACCCCA CTCCTCCTGC AGCCACTCCC 1440 TGTGCTCCCC AGCCCCTGGC CCAGACACCT CCAGCTGCCT CCAGACTGGG TCTCCTCCCA 1500 AACAAAGCCG GATTCAGGCC TTCGGGAGGC AGGCGCGCAG GTTCTGCCAT GGAGATGAAC 1560 TTTGACCCAA ACAGCAAGGC TCCTACCCCT TATTTACTCT TTAAGGCTGA CCCGTTTCAC 1620 AGAGTTCACA TTACACCCCT TTTTAATCCG CACCTCCCTC CCACATTCCA GGCCTCGACC 1680 TTCAACCCCT CCTAATTGCT GGCTCCGGCT CCTACACCCC AGTTCTTGGG CCCAGCTCAC 1740 TCATCCCTGC CCCCAACCAT CTCCTCCACG GAAACAAAGG CGATGCTGGG GTGCTGTGCT 1800 CACAGGGCCA CCTCACAACC CTGGCACACC AAGGTAGATG CCAGGGTCCC AGAGCCCAAC 1860 CACTTGGGGG AGTCCACGTG GAGGCCGGGG TGGATCTTTG GGGTCTGATT CCTGACCCTA 1920 ACTCTCCAAC CCCTGAGAAG GAAGCCTCTA TTCCAAGGGA GGCTGGAGTA GGCTGCCTGG 1980 CAGGCCCTGC GCGGAGGCGG TCAGGGCTAG GGAAGAATCC GGACAGCTCC CCAGCCAGCC 2040 GCATCGCATC CCAAGGGGCT AGGGTGAATG TGGGCAGCTG CACTGCCTGG TCACTCACCA 2100 GGTGACCTGG GCTATAGCCT CACATGTGGC TGCAGAAACA CAGCTTGTTT CCCTTGCTGG 2160 GCAGCGGAAC TGCTCTGGGT TAGGTACACT GTGAACCTTC CCAGGCCTGC CCCTGGTAAC 2220 TCTGAAACCC ACATTGCAGA AGCCCATGGC ATCCCGGCAA CCAGGCAGAC CCCCCGCCCC 2280 GCAGGCTGCC AGTCCTATGG GCTCTCTCCC TCATCTTTGG GAGGAAGGAG CCAGGAGCTG 2340 GGGCACTGGG GCCCATGGAG ATGCTGAGAA CACTGGGGGC AGTGCAAGCT TGGGCCTGAG 2400 CCACCCAAAG GCCTTGGCCC AGATTCCGCC ACCCTGGAGT GTGTCCACAC CTCTCACCTG 2460 AGGACAACTG GGAGCAGGGG GCCGGGCACA GCCCCTCCTC AACTGCCACC AAGGGGCACT 2520
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