Tag | Content |
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EnhancerAtlas ID | HS085-00615 |
Organism | Homo sapiens |
Tissue/cell | Heart |
Coordinate | chr11:75022510-75024010 |
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 | TGAAGCACAA TGAAGAGTTT GTCAGATTGT CAAATTGCAG AAGAGAACGT TAAAGGAACA 60 GGCTATGCAT GGAATGCACA TCCTTACATA GCAGACTGCA CATTTCAAAA ATCAGTTCAA 120 AATCACAATC TCGTTTCACC CTCTCAAATC CCATAATGGT GTTATTAACT GCCTCTCCCA 180 CGGCCCTCCA CCTGCCACAC ACAGGCAAAC AAAAAAAGTA AGGTCCAGTG AAGGCAGATG 240 GTGAGCCCCA GGGCAAACAA ACGGTGACTG ATTTCTGAGT AGAGGGAAGT GAGGGGTGGA 300 CTCTGGCTGA AATGGTCCTC TTCTCACTGA AGTGGGGGAT TCCTGAATTC CTGTCCGGCG 360 GCAGCACCCC ACTTCGGCCC CTGCTGGCCT GTGACACCCT CCTCTCATCC CCAGCATACA 420 CACACACTCC TCCGGCCACC AGGGCCTGTC AGAAGGGGCT GGCTGAGAGG GGACGGCCGG 480 CAGAGGAACC AAGCAGCAGG GCCTGGGCCG AGGGGCTGGG AAAAAGCTGA CCGTTCTCGA 540 AGGCCCAGAT CGGAGGCCCT GCCCAGCCTC TTCCCCTCCT CTAAGTGCTG ATCACCTCAG 600 CCTCTCCCGC TGCAAGTCTC CTTCCATGGC CTCTCCTCTC CCATCTCTTG CAGTGGCTGC 660 TGCTGGCCTC TCCCTTCTCC TTCCTCCACC CTCGCCCTCC CCGGGGAGTG GTGAGCTCAG 720 CCTTTCCCAG CAGCCGTCCC TAGGAATGAT GGGAAATGCA CCGCCAGGAA CTGAGAACAG 780 GCCTGCCCCT GGGAAGGAGT GGGAGAAGAG GCGTCAGGGA CAGGGCTCAA GTCTGCCACT 840 TCCTAGGACC CCTGACCGCC GAAGGGACAG TCTGCCTGTG TGTACTGCAC GCTGGAAGGA 900 CATGGGCTCA GACTGTGTGG ACTGCCAGGG ACCTTGTCTT ACAGATGGGG AGACAAAGGC 960 CCCAGGAGAG GAGAAAGGGG ACTGACTGCC TGTCCCAGGC ATTGGGAGCC TTTCATTGTC 1020 TCATGTCATC CTCACAACTG CTCTGCAAGG TGTGTGTGGT AGGCTGAGTA ACAGCCCCCC 1080 GAGATGCCCA CATCCTAATC ACCAGAGCTG TGGCTGTGTT GGGTCATGTG GTAGAAGAGA 1140 TTCTGCAGAT GTGATTTTGT TCAGGGCCTT GAGATGGAGA GATTATCCTG CATGACCTGG 1200 GTGGGCCCAA TGTCATCACA AGGGTCCTGA CAAGAGGGAG GCAGGAGGGT CAGAGAGAGT 1260 AAAGGCAATG GGGTGATGGA AGCATTGAAA GACAGACGAA AATCTACACT GCTGGCTTCA 1320 AAGCTGGAGG ATGGGGCTGG GAGCCAAGGC ATGCAGACAG CTTCTGGAAG CCAGCAGAGG 1380 CAAGGGAATG GATCCCCGCT AGAGTTTCCA GAGGACACAG CCCTGACAAC CCATTTCAGG 1440 ACTTTGGACC TCCAGAAGTG TAAAGAATAT ATTTGTGTTG TTTTAAGCCA CTAAATATAT 1500
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