Tag | Content |
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EnhancerAtlas ID | HS040-07081 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr11:75022380-75023920 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SREBF2 | MA0596.1 | chr11:75023777-75023787 | ATGGGGTGAT | + | 6.02 | TFAP2C | MA0524.2 | chr11:75022753-75022765 | AGCCCCAGGGCA | + | 6.11 | ZNF263 | MA0528.1 | chr11:75023176-75023197 | CCTCTCCCTTCTCCTTCCTCC | - | 6.86 | ZNF263 | MA0528.1 | chr11:75023179-75023200 | CTCCCTTCTCCTTCCTCCACC | - | 7.29 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_00135 | chr11:75016201-75027347 | Adipose_Nuclei | SE_03287 | chr11:75022298-75024209 | Brain_Angular_Gyrus | SE_04031 | chr11:75020093-75025864 | Brain_Anterior_Caudate | SE_04951 | chr11:75011977-75027109 | Brain_Cingulate_Gyrus | SE_05927 | chr11:75011975-75026931 | Brain_Hippocampus_Middle | SE_07122 | chr11:75020120-75026037 | Brain_Hippocampus_Middle_150 | SE_07907 | chr11:75011958-75027094 | Brain_Inferior_Temporal_Lobe | SE_13386 | chr11:75022344-75023722 | CD34_Primary_RO01536 | SE_23271 | chr11:75022374-75023957 | Colon_Crypt_1 | SE_24003 | chr11:75022650-75023773 | Colon_Crypt_2 | SE_25192 | chr11:75022381-75023965 | Colon_Crypt_3 | SE_25898 | chr11:75021122-75025829 | Duodenum_Smooth_Muscle | SE_26962 | chr11:75022396-75025702 | Esophagus | SE_28109 | chr11:75022444-75023821 | Fetal_Intestine | SE_29208 | chr11:75022428-75023853 | Fetal_Intestine_Large | SE_31429 | chr11:75022250-75025778 | Gastric | SE_42220 | chr11:75019878-75027219 | Lung | SE_46889 | chr11:75022715-75023607 | Ovary | SE_47208 | chr11:75022351-75024084 | Panc1 | SE_50175 | chr11:75022398-75024164 | Sigmoid_Colon | SE_52494 | chr11:75022371-75025749 | Small_Intestine | SE_53599 | chr11:75022306-75025821 | Spleen | SE_54712 | chr11:75022246-75025882 | Stomach_Smooth_Muscle | SE_65484 | chr11:75021917-75025888 | Pancreatic_islets |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH11I075311 | chr11 | 75022321 | 75025870 |
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Enhancer Sequence | AAGAAAATAT AAAAATTAAA AAAATTAAGA GGCCACAGCA ATTCCGAGAA AGGAGCAGCT 60 CCATTCTTTC TGGGATGGGC AGGGGGCTGT TGAGAAAGTT GCAGAGAGCA GGTGACATCT 120 GAGCTGGACT TGAAGCACAA TGAAGAGTTT GTCAGATTGT CAAATTGCAG AAGAGAACGT 180 TAAAGGAACA GGCTATGCAT GGAATGCACA TCCTTACATA GCAGACTGCA CATTTCAAAA 240 ATCAGTTCAA AATCACAATC TCGTTTCACC CTCTCAAATC CCATAATGGT GTTATTAACT 300 GCCTCTCCCA CGGCCCTCCA CCTGCCACAC ACAGGCAAAC AAAAAAAGTA AGGTCCAGTG 360 AAGGCAGATG GTGAGCCCCA GGGCAAACAA ACGGTGACTG ATTTCTGAGT AGAGGGAAGT 420 GAGGGGTGGA CTCTGGCTGA AATGGTCCTC TTCTCACTGA AGTGGGGGAT TCCTGAATTC 480 CTGTCCGGCG GCAGCACCCC ACTTCGGCCC CTGCTGGCCT GTGACACCCT CCTCTCATCC 540 CCAGCATACA CACACACTCC TCCGGCCACC AGGGCCTGTC AGAAGGGGCT GGCTGAGAGG 600 GGACGGCCGG CAGAGGAACC AAGCAGCAGG GCCTGGGCCG AGGGGCTGGG AAAAAGCTGA 660 CCGTTCTCGA AGGCCCAGAT CGGAGGCCCT GCCCAGCCTC TTCCCCTCCT CTAAGTGCTG 720 ATCACCTCAG CCTCTCCCGC TGCAAGTCTC CTTCCATGGC CTCTCCTCTC CCATCTCTTG 780 CAGTGGCTGC TGCTGGCCTC TCCCTTCTCC TTCCTCCACC CTCGCCCTCC CCGGGGAGTG 840 GTGAGCTCAG CCTTTCCCAG CAGCCGTCCC TAGGAATGAT GGGAAATGCA CCGCCAGGAA 900 CTGAGAACAG GCCTGCCCCT GGGAAGGAGT GGGAGAAGAG GCGTCAGGGA CAGGGCTCAA 960 GTCTGCCACT TCCTAGGACC CCTGACCGCC GAAGGGACAG TCTGCCTGTG TGTACTGCAC 1020 GCTGGAAGGA CATGGGCTCA GACTGTGTGG ACTGCCAGGG ACCTTGTCTT ACAGATGGGG 1080 AGACAAAGGC CCCAGGAGAG GAGAAAGGGG ACTGACTGCC TGTCCCAGGC ATTGGGAGCC 1140 TTTCATTGTC TCATGTCATC CTCACAACTG CTCTGCAAGG TGTGTGTGGT AGGCTGAGTA 1200 ACAGCCCCCC GAGATGCCCA CATCCTAATC ACCAGAGCTG TGGCTGTGTT GGGTCATGTG 1260 GTAGAAGAGA TTCTGCAGAT GTGATTTTGT TCAGGGCCTT GAGATGGAGA GATTATCCTG 1320 CATGACCTGG GTGGGCCCAA TGTCATCACA AGGGTCCTGA CAAGAGGGAG GCAGGAGGGT 1380 CAGAGAGAGT AAAGGCAATG GGGTGATGGA AGCATTGAAA GACAGACGAA AATCTACACT 1440 GCTGGCTTCA AAGCTGGAGG ATGGGGCTGG GAGCCAAGGC ATGCAGACAG CTTCTGGAAG 1500 CCAGCAGAGG CAAGGGAATG GATCCCCGCT AGAGTTTCCA 1540
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