Tag | Content |
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EnhancerAtlas ID | HS105-15204 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:75022730-75023840 |
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 | AGGTCCAGTG AAGGCAGATG GTGAGCCCCA GGGCAAACAA ACGGTGACTG ATTTCTGAGT 60 AGAGGGAAGT GAGGGGTGGA CTCTGGCTGA AATGGTCCTC TTCTCACTGA AGTGGGGGAT 120 TCCTGAATTC CTGTCCGGCG GCAGCACCCC ACTTCGGCCC CTGCTGGCCT GTGACACCCT 180 CCTCTCATCC CCAGCATACA CACACACTCC TCCGGCCACC AGGGCCTGTC AGAAGGGGCT 240 GGCTGAGAGG GGACGGCCGG CAGAGGAACC AAGCAGCAGG GCCTGGGCCG AGGGGCTGGG 300 AAAAAGCTGA CCGTTCTCGA AGGCCCAGAT CGGAGGCCCT GCCCAGCCTC TTCCCCTCCT 360 CTAAGTGCTG ATCACCTCAG CCTCTCCCGC TGCAAGTCTC CTTCCATGGC CTCTCCTCTC 420 CCATCTCTTG CAGTGGCTGC TGCTGGCCTC TCCCTTCTCC TTCCTCCACC CTCGCCCTCC 480 CCGGGGAGTG GTGAGCTCAG CCTTTCCCAG CAGCCGTCCC TAGGAATGAT GGGAAATGCA 540 CCGCCAGGAA CTGAGAACAG GCCTGCCCCT GGGAAGGAGT GGGAGAAGAG GCGTCAGGGA 600 CAGGGCTCAA GTCTGCCACT TCCTAGGACC CCTGACCGCC GAAGGGACAG TCTGCCTGTG 660 TGTACTGCAC GCTGGAAGGA CATGGGCTCA GACTGTGTGG ACTGCCAGGG ACCTTGTCTT 720 ACAGATGGGG AGACAAAGGC CCCAGGAGAG GAGAAAGGGG ACTGACTGCC TGTCCCAGGC 780 ATTGGGAGCC TTTCATTGTC TCATGTCATC CTCACAACTG CTCTGCAAGG TGTGTGTGGT 840 AGGCTGAGTA ACAGCCCCCC GAGATGCCCA CATCCTAATC ACCAGAGCTG TGGCTGTGTT 900 GGGTCATGTG GTAGAAGAGA TTCTGCAGAT GTGATTTTGT TCAGGGCCTT GAGATGGAGA 960 GATTATCCTG CATGACCTGG GTGGGCCCAA TGTCATCACA AGGGTCCTGA CAAGAGGGAG 1020 GCAGGAGGGT CAGAGAGAGT AAAGGCAATG GGGTGATGGA AGCATTGAAA GACAGACGAA 1080 AATCTACACT GCTGGCTTCA AAGCTGGAGG 1110
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