Tag | Content |
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EnhancerAtlas ID | HS159-00096 |
Organism | Homo sapiens |
Tissue/cell | Pancreatic_islet |
Coordinate | chr1:21638860-21642080 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BARHL2 | MA0635.1 | chr1:21640493-21640503 | GCTAAACGGT | + | 6.02 | MEF2B | MA0660.1 | chr1:21639333-21639345 | GCTAATAATAGC | + | 6.07 | MIXL1 | MA0662.1 | chr1:21640589-21640599 | TCTAATTAAC | + | 6.02 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_00105 | chr1:21640019-21654616 | Adipose_Nuclei | SE_00854 | chr1:21639451-21641453 | Adrenal_Gland | SE_00854 | chr1:21641602-21642092 | Adrenal_Gland | SE_01643 | chr1:21639425-21641555 | Aorta | SE_02944 | chr1:21640912-21641449 | Bladder | SE_04518 | chr1:21639355-21640025 | Brain_Anterior_Caudate | SE_05710 | chr1:21639125-21641783 | Brain_Cingulate_Gyrus | SE_05944 | chr1:21639044-21646536 | Brain_Hippocampus_Middle | SE_08398 | chr1:21639007-21640675 | Brain_Inferior_Temporal_Lobe | SE_26127 | chr1:21639824-21641988 | Duodenum_Smooth_Muscle | SE_26770 | chr1:21639500-21641528 | Esophagus | SE_28486 | chr1:21639904-21640821 | Fetal_Intestine | SE_31433 | chr1:21639359-21640599 | Gastric | SE_31433 | chr1:21640646-21641344 | Gastric | SE_42174 | chr1:21639360-21640363 | Lung | SE_44380 | chr1:21639052-21642110 | NHDF-Ad | SE_45045 | chr1:21639124-21641481 | NHLF | SE_46660 | chr1:21639608-21640018 | Ovary | SE_46660 | chr1:21640643-21641290 | Ovary | SE_47592 | chr1:21639448-21639851 | Pancreas | SE_48583 | chr1:21639382-21641534 | Right_Atrium | SE_50108 | chr1:21639410-21641515 | Sigmoid_Colon | SE_54639 | chr1:21639148-21648300 | Stomach_Smooth_Muscle | SE_56171 | chr1:21639209-21642705 | u87 | SE_65263 | chr1:21639302-21641232 | Pancreatic_islets | SE_67931 | chr1:21639209-21642705 | u87 | SE_68932 | chr1:21639403-21641393 | 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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| Number: 1 | ID | Chromosome | Start | End |
GH01I021312 | chr1 | 21638973 | 21657659 |
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Enhancer Sequence | GGCTGAGGCT GCAGTGAGCT GTGATTGCAT CCCTGCACTC CAGCCTGAAA GACAGAGTAA 60 AATCCTGTCT CAAAAAAATA ATTTTAAAAA TTTAAAAAAT TAGCCTGGTG TGGTGGCACA 120 CACCTATCAT CCTAGCCACT CAGGAGGCTG AGGCAGGAGG ATCGCTTGAG CTCAGGGAGG 180 TCAAGGTTAC TGTGAGCTAT GATTGCGCCA CTTCTCTCTG GCCTTAGTGA CAAAGCAAGA 240 CCCTGTCTCT TAAATAAATA AATAAAAAGA GCAAGCAGCA TCCCCAGCTG ACACAGCACG 300 TGTCCCATGT GCTGTCCTGT CACTGAGAGG TAGGAGGATG CAGCAGGCTG GAGTGTGGTG 360 GACATGGGTC TATACCGCCT GTATTCAAAT CCCAGCTCTG CCTACTACTA TTTGTTTGAC 420 TTGGGCAAGT GATATGACCT CCCTGTGCCT TGGTTTATCA TTAAAAAAAC AAAGCTAATA 480 ATAGCCCCAC TCTCATAGGT AGCTATGAGA ATTAAAATAG TTCAAAGACA CAAAGTATTG 540 TGATCACCAG CACTGCTATT TGATCCTCTC ATGCAGATGT AAGGTAAATA CTATCATTGT 600 CTCTCATTTT GCAGATGCTA AAACTGCAAC TCAGAGAGGG GTAGTGACTT GCTTGGATCA 660 CACAGCCAGA AAGTGACAGG GCAGGACTGG ACACCAGGTC TGTCTGACTC TAAACTACTT 720 ATTGTTTCCA CTCTGCCCTC TGCGCCCCAC TATTCCCTCC TGGACTCTGA TGCCTCTGTG 780 CTTGTCCCCT CACCTGCCCA CAATGCCAAG GCCAACTCCC CTTGTCTAGC CCCAGCCAAT 840 CAGGGTGGAC CTGCAGCCAA ACCAGATGCT GCTGAGCTGG CGTTGCCTCG GTGACCAGGC 900 ATATCTGCTG GACAAGCCCA CCCCAGGCTC AGCTTCCCAT CTGGTCCCCA GTACACTCCA 960 TCCCCCTCAA GACACATGTG TCATGCTTGC CTGGGGGGAT GGAGGGAGCC CGGGAGGAAA 1020 CGCCTGGCTG GGGAGAGGAG GGCTGATTCC AGCTGACAGT GGGGGAATGA TGACTGCATT 1080 GGCTCAGGAG GACAGGAGCT GCCCTAGCTG CAGTCTTGGT CCAGAGTGGT CCCAGGCCCA 1140 GAGCAGAGCT GGGCGGGGAT GAGAACTAGG GAGAGGAATA CATGATGCAG GTGGGAGTGG 1200 GGGAGCAGGG GGCTGAGCAC CAGGCTCAGA TCCAATGAGA ACAAGCTGCT CCCTCAACCT 1260 TGGAGTGGAA AGAACAAAGG TTCTGGAACA GACAGACCTC AGCTGGACTC TCTGTAATTT 1320 ACTGCTGTGT GACCCTGGGT GAGTTGCCTT ACCTCTCTGA GCATGTGTTC TCATCTATAA 1380 AATGGGGACA TGTGAACCTA CTTCACTGGG CTATGGTGGG AATTAAGGCG ATAATCCATG 1440 AAAAGGCACA TGGGGAATTC AAGTGCTGCC TCCTAAAGAG AGGCACTGCC AAGGTAATGC 1500 CTGTGGCACA GGAATGTCCC GGCTCACGGA GAACGGGTAC GAGCAGCTGG AATGACCCTG 1560 GGTTCAACCT GAGCAGTAGT GTGGCCTGGG TTACAGATGT AGGGGCAATG ATGACAGTGC 1620 TGAGGCTGCA GCTGCTAAAC GGTAACACCA ACGACATGGC ACCAGCAAAA GCCACATCTT 1680 GAGCAATGAC TTCATTCTAG GTTCCGTGCT AAGCACTTTA CGTGTGTTTT CTAATTAACC 1740 ATAACAGCAA CCCCACGTGA AAGATGTGGA ATAAGAGACA CAGAGAGGTT AAGTAACAAG 1800 TCCAAGGTTG CACAGCTGGT AAAAAGATGG GATCAAATTT GAACCCAATT TCTACCCGAT 1860 ACTCAGGCAT TATGGGAGCC TGCAGAATGG CGTGGGAGTT CTGGGAAGGG GGCGCTGGCT 1920 AGGCCCTTCC TGGGACACTC ACGCAGCCAC ATTCCCAAAC CCCCTCCCGG GCCCCCAAAT 1980 TCCTGGCTCG GTAGTGATAC AGCCTGAGCT CCTCCTCTCC CTCCAGGGCT TGGCTCAGTT 2040 CAGTCCCATT CGGGAGCCAA TCTGCCATTG CACAATTAAC AATTAGGAAC AACTTTTCTT 2100 TTCTTCCAAG GCAGGGATCG GCCCCAGCCC TGGTGACAGG GACACAGTGG GGCTTCTGAC 2160 AGAACCTACT AGGTATGTCC CCAGCCCCTT GCCAAGCTGG GTGACCCCTT TCCTAACCCA 2220 GCCCAGTCAG GAAATCAAGG GTCAGACAGC CCCTCTCCAT CTTCCTTTGT CATCTAAATC 2280 CAACCTCCCC TCCAGGGAAC TTCCTGACTG TCCTGGCTCA CAGCTTTCAC GTGTTCCTAA 2340 GACCCCAACG CCACTGATTC TTTGTCTATT CAGTCAGTAC CTGGCCTGTG CCATTTCCAT 2400 GGGATCATGT ATCTTTATCT ACTGCAAGCA ACTTGAGTTT GTTTGTTGTT GTTTTTGTAA 2460 ACAACACTGT GCTTATCCCT CTCAATACCA AATCTAGTCC AGGACGCATA GAAACTGTTT 2520 GACCTATGGT CTGCTTCTTG GCTTGGAGAA CTCCTATTCA CCCTCCAAAA CCCAGATGAA 2580 ATGTCATCTC CTCTATGAAG TCTTCCTCTG TGTCCCATGC TGCCCCATCT GTATGTATCT 2640 GTAGTGATTT GTATGTATCC CCAGTAGAAA ACCCTCCCTT GTACTGTAAT TAATAACTAC 2700 TATCCAGGCA CTGTGTTAAG ACTGTCACAC TCATTAATTT CAAATCTATC TCTCTGCAAG 2760 CCAGAGTCAA TACCTATTTA ACAGATGGGG GTGATAAGGC TCAGAAAGGT TAAGAGGCTT 2820 GCCTAAAATC ACACAGCTAA TAAGTGGCAG ATCTGTAATT TGAGCCCAGG TCTGCTCATG 2880 TCCCAAGCAA ATAATTCTTT GGTTGGTTCA GGCTGCCACC TCCATCCAAC TGCAGCTGAA 2940 TCCGATGCCT ACTGGGGTCC CAACCTTTGC AGTTCCCCAA TGGATCAACC TCAGAGATGA 3000 GCTGTCACTC AGCCCCAATG TCTGGGGTAT CCCAGGCCAA AGGTGATCTA CCAGCTGGTG 3060 CCACCTCACC CTCACGGCGT CTAGGACAAC CTGGAAAGTC CTAGGGGCTT GTATATAGGC 3120 AACTAGGCAT TAAAAGCTGC TCCTGGCCGG GCATGGGGGC TCAGGTTTGT AGTCCCAGCA 3180 CTTTGGGAGG CCAAGGCAGG CAGATCACTT GAGGTCAGGA 3220
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