Tag | Content |
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EnhancerAtlas ID | HS127-30443 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr8:67433540-67436720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr8:67434868-67434883 | GGGGCAAGCTGACCT | - | 6.79 | Foxd3 | MA0041.1 | chr8:67434919-67434931 | AAACAAACATTC | - | 7.22 | Twist2 | MA0633.1 | chr8:67434272-67434282 | AACATATGGT | - | 6.02 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_01716 | chr8:67429742-67436254 | Aorta | SE_01716 | chr8:67436257-67436719 | Aorta | SE_02451 | chr8:67433314-67436204 | Astrocytes | SE_03311 | chr8:67433479-67436032 | Brain_Angular_Gyrus | SE_04061 | chr8:67430640-67436433 | Brain_Anterior_Caudate | SE_04954 | chr8:67429436-67437004 | Brain_Cingulate_Gyrus | SE_05993 | chr8:67429348-67436398 | Brain_Hippocampus_Middle | SE_06856 | chr8:67433061-67436877 | Brain_Hippocampus_Middle_150 | SE_07872 | chr8:67429503-67436499 | Brain_Inferior_Temporal_Lobe | SE_08914 | chr8:67434546-67435869 | Brain_Mid_Frontal_Lobe | SE_20725 | chr8:67434200-67435972 | CD56 | SE_36142 | chr8:67433124-67438712 | HMEC | SE_37326 | chr8:67433029-67437102 | HSMMtube | SE_38764 | chr8:67433389-67436357 | HUVEC | SE_41451 | chr8:67429480-67436697 | Left_Ventricle | SE_43305 | chr8:67429741-67436164 | Lung | SE_43493 | chr8:67429918-67438662 | MCF-7 | SE_44736 | chr8:67433000-67436682 | NHDF-Ad | SE_45011 | chr8:67433006-67436334 | NHLF | SE_45855 | chr8:67428834-67436952 | Osteoblasts | SE_47153 | chr8:67419159-67438708 | Panc1 | SE_49256 | chr8:67429893-67436269 | Right_Atrium | SE_51745 | chr8:67433246-67436747 | Skeletal_Muscle_Myoblast | SE_54868 | chr8:67429551-67438280 | Stomach_Smooth_Muscle | SE_56182 | chr8:67433214-67436443 | u87 | SE_63533 | chr8:67433188-67436780 | HSMM | SE_65207 | chr8:67433428-67436325 | NHEK | SE_68177 | chr8:67418890-67478365 | TC32 |
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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 |
GH08I066516 | chr8 | 67428306 | 67440606 |
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Enhancer Sequence | CATAAGTAAC AGGCAGGCTA AGATAGAGAG GGATCACCCC TTAAACTGTC ATCAGTCATT 60 TATGCCTTAG AGTAAGTGAA TGAAGGAATG GAGAGGAGGT TTTCGTAGGG ACTGGCAGGT 120 AAGGGGAAAG GAAGGAGGTG TAATACCAAG GGAAGGAAGT GTTAGGAGCC CAAATGGGGA 180 AACAACTTCA GGCTATTTCT CCTCACTGCC TAGAGCCCTA CTTATCCTCC AAGCCCTACA 240 TGTTCCCCAC CAGCATTTTA AATTCCTTGG ATTCAAGGTG CAATACTCCC TGGAAGCAGA 300 TGTCCTCCAT GAAGAAGAAG GGAAATGGGC CCCACAGGTG GTGCTGCAGA GTCCCACTCG 360 CCAGCCACGG ACACCACGGA CACCCAGGAC AGTGTAGACG GGTGGGACAA TGGACCCTGG 420 ATGGTGAAGG AGCACCAGAT TCAAGGCAGA ATGCCTGGCC CCAAGACTCA GCCCCACACT 480 TACTGGAGAG AGAGAGAGAG AGAGAGAGAG AGAGAGAGAG AGAGAGAGAG AGAGAGAGAG 540 AGAGAGAGAG TGTGTGTGTG TGTGTGTGTG TGTGTGTCAT TGGTCAAGCT GCCTGAGTTT 600 CTTTGAGTCT CTATTTCCCC TCATCTGTGA AATGTGGATT AAATTACCTG CCCAGCCAAC 660 CTCACAGGCT GATGAAAGAT CAGAAGAGAG CTGGTGTATA AAAGGACTTT GTAAATTGTG 720 AATTGCACTT CTAACATATG GTGTTATGCT AATCCACTCC ATTCAGAAAG AAGCAGATCT 780 GGGCGTGGGG AGAAGTGACT CAGGCAGCTG AAGACAGGAG TGAGGGCTGA AAAGCTAGGC 840 GGTGACTGAA AATAGAACCG TTTTCAGAGC TCCCGTGCCA GGTTCCTGGG ACCGGGCTCG 900 CCAGCAGCTG GCAGGCAGGG GCTCCAGGCT GGCCAGGCCC CAGCTACCTG CTCCCCAGTG 960 CTGCAGCCCG AGGTGGCCAG ACGCCCCACC TGGTCAGTGC AGTCCAGCGA CCTCTGCTCA 1020 CAAGCAAGAA GTGGAGGATG AGGACCAGTT TTTTGAATTC AAATGACTCT CTCTCCTGGA 1080 GCCGCCTGCT TGCTGCCAAA TGCAGCTTTT GGCTTCTTGC CTGCATTCCT ACCAGCAAAA 1140 TTAGCCCACA GATGAAACCT ACAAAGCACA TTGGCCCAGG AGACCAGAGG CCCTGCCTGC 1200 ATGCTCCAGC CCCACGAGGG AAGTGTCCCC TGCCCATCCT GCCTTAGCTG AGCCCCAGCC 1260 CTCCTATTTT GAGGCAGGTA ACAGGGCCGG TACCCACAGG ACTAAGCACT ACTAAGCCAT 1320 CAAGGTCCGG GGCAAGCTGA CCTGTGTGGG TGTAACTAGG CACAGACTTG ATGTTTCATA 1380 AACAAACATT CCTTCAAGGC ATTTCTGCTG CTAGCTCAGG CCAAGGAAAG CAAGGTAATA 1440 ACTCAAGGAA CAGTGACCTC ACCAGGAAAG CAGGCTCCTC AGTCTCACAC ACAAATCCCA 1500 CATCCCCATA TATCCCAGAC TCAGTGTGTC ATGAAAAATC CCCAAGAGGC ACTCCCCTGT 1560 AAAGGGAGCA GGTAGCCAGT TGAGAAGCAG GCTGGGAGCA GGGAGGGAGC TTTTTTCCAG 1620 CTGCCTAGAG ATACCACCAT CTCAGGAGCA AGGAGTGGGC AGTGCAGAGG GTCTCTGCCC 1680 TCTGTGGGTC CTGCCCTCTT GCCACCACAG AAAGAAAGCA GAACAAAGCC GAAACTATTT 1740 GTCATTTTGG CTCTTTCAGG TCCTGGCCAG GCTCTGTGAC AGCATGCTGC CTCGGCAGCC 1800 ACTGGGAGCT GGAGCTGGAG CTGGGAACTG GGAGCCAAGC ACTGGGCCCT GTTGTGAAAC 1860 CACTCAGCCT GGTCCTGTTT CATTTCCCCC ATCTGCTGCT TTGTTCTTCC TCAGGATGTG 1920 GTGAGAGGTG GAGACTGGGG AAGGAAGTAG GAAGAAGAGA GGCCTGGAAG TCCTGGCTGT 1980 TTATTCCCTG ATCCTCCACC CTGAGAAGAG AGAGGGCAGA AAGCCACCCT GTCTCTGAAC 2040 CTGGGTAAAT GCACCCCCCA GGTACCCACC TGTGTGCTGG AGGCTACTTG AAGCTACAGG 2100 CTAAACCCAC ACATCTTCCT GGGCCCTCCA GTTGGGCCGC AGTGGACTTT AACACATTAA 2160 GACAAATACA ACTGTATTAA CAGAAGCTAA CATTTATGCT TTACATGTGC TGGACACTGT 2220 GCTAAGTGCA TCAAGTACCT CAGCTCATGC AATCCTCCAA ACAACACCAT GGGATGGCTC 2280 TTTCATTTAC CCTATTGGTT TACAGAGGCT TAGAGAGTTC ATGAGGTTGC TTGAGGTCAC 2340 ATAGCTATGG GTGGCGGCCC AGAGATGGAC TCAGGCAGTT GGACTGCAGA GCCCACTGCA 2400 GGTAGATGTC CAATTTGTAC ACTGCCCGAA GGTGCCCTAC TAGCGACAAG TACTGTGTGC 2460 ATGGGCACTG CCTCCACTCA AAGACAGCAC TGTCCACTTG CTTCGAGGGG TCAGCTTCCT 2520 AAAGTGGCAA AATTCACTTG AATATTTCAG TTAAAAGTTG AGTTCTCTTT GGCAGTGTTA 2580 GTATCAAAAC ACCAATAGCT ATATGTAACT ATGTAACTAT ATGTAACTAG TTATATACAT 2640 ACACTCTATA ACTATATGTA ATTGTTATGT AGTCATATAA TTACATATAG TTATTGGTGT 2700 CATGGTACTA ATTTAATATT CTGTTAAATT GAGTTAAATT GAGTTTAGCC TAAAGCTGCC 2760 TCCTTACATC TTCCTAAAGG TTTCTCCCTA CACAGTGAAC TGTACCCTAA ACTGGACGTA 2820 TAAACAGACT GTAACCTACT CTTGTTTCAG CCCGTCACAG ACGGCCAACT GTTCGTACTG 2880 TGTTCAAGTA AGGCAAAAGC CCAGCTGTAC CCTGTGCAGC TGTACCAGGC AAGAATCCAG 2940 CTGTGTCTGG TCCTCACTCC CACTTTCTGT ATATCACTTT CCTTTTTTCT CTCCATAAAT 3000 GCCCTCCGAC CACACAGCAA TACCAATAGA GTCTCTCCAA ACCTATTCTG GTGTGGAGGA 3060 CTGCCCGATT CACAAACAGT TTTTTGCTCA ATTAAACTCT GTTAAATTTA ATTTGTCTAA 3120 AGTTTTTGTG TTAACGCCTT CAATTTCAGC CCCTTTCTCA AAGGTCACCG CTACTATCAA 3180
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