Tag | Content |
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EnhancerAtlas ID | HS017-21333 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr21:39616280-39619250 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr21:39617621-39617639 | GAAAGGAAAGAAAGAAAG | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr21:39617516-39617534 | GAAAGAAAGAAAGGAGGG | + | 6.09 | EWSR1-FLI1 | MA0149.1 | chr21:39617543-39617561 | GAGAGGAAGGAAGGGAAG | + | 6.25 | EWSR1-FLI1 | MA0149.1 | chr21:39617650-39617668 | GAAAGGAAGGAAGGAGAA | + | 6.46 | EWSR1-FLI1 | MA0149.1 | chr21:39617520-39617538 | GAAAGAAAGGAGGGAAGG | + | 6.98 | EWSR1-FLI1 | MA0149.1 | chr21:39617528-39617546 | GGAGGGAAGGAAGGAGAG | + | 7.58 | EWSR1-FLI1 | MA0149.1 | chr21:39617524-39617542 | GAAAGGAGGGAAGGAAGG | + | 8.69 | GLI2 | MA0734.2 | chr21:39617787-39617802 | AGACCACCCACAAAG | + | 7.02 | GLIS3 | MA0737.1 | chr21:39617788-39617802 | GACCACCCACAAAG | + | 6.26 | HNF1A | MA0046.2 | chr21:39618019-39618034 | AATTAATAATTAAAT | + | 6.58 | IRF1 | MA0050.2 | chr21:39617639-39617660 | AGAGAGAAAGAGAAAGGAAGG | - | 6.44 | ZNF263 | MA0528.1 | chr21:39617544-39617565 | AGAGGAAGGAAGGGAAGGGAA | + | 6.25 | ZNF263 | MA0528.1 | chr21:39617545-39617566 | GAGGAAGGAAGGGAAGGGAAA | + | 6.2 | ZNF263 | MA0528.1 | chr21:39617659-39617680 | GAAGGAGAAAGAGAATGAAAG | + | 6.36 | ZNF263 | MA0528.1 | chr21:39617537-39617558 | GAAGGAGAGAGGAAGGAAGGG | + | 6.45 | ZNF263 | MA0528.1 | chr21:39617533-39617554 | GAAGGAAGGAGAGAGGAAGGA | + | 6.94 | ZNF263 | MA0528.1 | chr21:39617525-39617546 | AAAGGAGGGAAGGAAGGAGAG | + | 6.99 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_09241 | chr21:39616014-39619090 | CD14 | SE_45623 | chr21:39615784-39618542 | Osteoblasts | SE_51700 | chr21:39615831-39618527 | Skeletal_Muscle_Myoblast | SE_55658 | chr21:39611717-39618807 | u87 | SE_63489 | chr21:39615519-39618707 | HSMM | SE_67472 | chr21:39611717-39618807 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr21 | 39616792 | 39617335 | chr21 | 39618516 | 39618880 |
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| Number: 2 | ID | Chromosome | Start | End |
GH21I038246 | chr21 | 39618516 | 39618880 | GH21I038244 | chr21 | 39615930 | 39618220 |
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Enhancer Sequence | AAGCTCTAAA AATACCAGGG AAGCAGGGAC CACGACACAT CCCAGGCTTG GTGCAGAAAC 60 CTGACCTGAA TTGGACCTTA AGATCAGAAT ATAGATCTAT TGTCTTTCCT CACCTGGCTG 120 TTACCAAACT AACTTCCGCA TCTCCTGGGA GTGCTTTCTA TTTCATCCAG GCAGTGCCCT 180 TATCTGATCT GGAGTGGGTT TATCTCTGGG AGAGCTATTG AAGTGCCTGA CAGGAGAGGA 240 CACTAAGAGT ACCTCCAGTC TCCAACTGCC TCCTCCGGCA GAACTGAGCA AGTCCTAACC 300 ATGCCAAAAA CATCATTATC TCTGGTTCCA TCTTAGTCCC TGCACACCCT AGGATTCAAG 360 GACTCAAGTA AGTTGGGGAG GGGAACATCT TTTCACCCCT GGAAAACCTT GTCTCCTCCC 420 AAGCCCTGGG AGGGGAGAAC TGCTGCTAAT GAGATGCTGG TAGTTAGTCT TGTAATTTTT 480 ACAGTATTAT CTGCAGAATG AATGACTACC AGCAGGTACT CTGAATCTCT TTTCTTTCTA 540 ATAAGATGTA ATCAACGAAC CAGATTGTGG CCTTGGAGCT GACCAAAGGA TCAGCTAAAG 600 GAATTGGACA CATCCTGAGC TAGTTAACAC ATGGGTATTG TCGGTCTAAG ATGCTCTTTA 660 GGGGCTAGTG ACTCATTCAT GATGTGCAGG AAATGGCACA GACACCTCCA TGACCACAGA 720 AGGTTTCTAC AGGCGCCGTC ATCACAGGGT CTACAAACAG AAGGAAGTCA GAGAGAGAGG 780 CTCAGGGGAA GGCAAGGCGG GGCTGGAGAC CTGGATTCTA CGTCGGAGTT TACCGCATCC 840 TGGTTCTATT CCCAAAGTCC TCTCTGTGTG GCCATATGCC TGATTCTCAG CCTGGCTTCA 900 TTCCAGTCAT CTCAGGATCT TACAAACAAC ATTGATGTCC AGGCCCCACC CCAGACCAAT 960 GAAATCAGAA TCTCTTGGAC ATTAAAAAAA AAAATGAGTG ATTCTTTCTG GGTGATTCTA 1020 ATATGTGGTC AGGGTTGAGG CCACTGCTTT ACTTCATTAC ATCATGACAC TAAAAATACT 1080 ACTGGAAAGA AAAAAGGAGG GCTACCATCT GCCTTCCAAT CTCTTCAGCT GGGAACCTCT 1140 TCATAAGACT GTATCTGAAA CCAGGATACG AGATCCTTAT AAGTAATTCC ATTTATAATA 1200 ACAAAGAAAG AAAAGAAAGA AAGAAAGAGA GAGAGAGAAA GAAAGAAAGG AGGGAAGGAA 1260 GGAGAGAGGA AGGAAGGGAA GGGAAAGAGA GACAGAGAAA GGAAAGAAGA AAGAAAGAAG 1320 GAAAGGGAAG AAAGAAAGAA GGAAAGGAAA GAAAGAAAGA GAGAGAAAGA GAAAGGAAGG 1380 AAGGAGAAAG AGAATGAAAG GTGTTTACAG CTGGAAATCA AACAGAACTT TGCCTGACAC 1440 ATGTTCATTT TTGGCCATTT TTGCCTTTTT TGTGGTGTGA ACCATTAGTT CAGCCCAGTT 1500 AACCCTGAGA CCACCCACAA AGACTGAATT CAGAGGTGGC TGTCCAGTAC AGTGATTCAA 1560 GGTGAGGCCT GTGAAGTGAG ATCAAGATTT GAATTTCTGC TTCTCAGTTC ACCAACTATT 1620 TGACCTTGGG CAAGTGACTT AATTCAAGAC TTAGTTTTAT CATTTATAAA GTAAGAAGAA 1680 TAATACCTGT CTTACATACT CTGATTTGTT GATATGATAG TCAATATGCT ATAAGAATAA 1740 ATTAATAATT AAATGACACG GTAGACATAA GGCATTTAAA TCTAATTCCT GATCCACAGC 1800 AAACCTTCAA CAAATAGCAG CTGTTATCAT CAGAGCTAAA ACGAATCATG TATCTAGGCT 1860 AGGGTCTGGT TTCTTTGCTG TTTTGGATAA TGGCTTAGGA ATAAGAATAA TGCCCACTGA 1920 AGAAGTCTTG ATTTTTCTTA AAGCTCTAAG CTCACTAGAG TTTTTTGCGT GTTGCCAATT 1980 TCAATCAGAT CCAGGAGTAT TGGTTACTGT TGGCCTATAT GATGAAGATT AACTTTTGGA 2040 AGAATCTTTC TGTGGAATGC AGGCCAAAAG AATTCTGAGG CTGCTTTTGA TTTGCTTTGA 2100 GTTCGTTGCA GCTAATGTGA AGGATGCAAA TATTTCTATA TTCCCTACTA TCTGCTTGGG 2160 GTCTTCAAGA GATGAGTTAC AGTGACCTGG AGGTAACATT TTAAAAATGC TAGTTAAGAT 2220 TAGTGTTAAA AACACAGACA AAGTCTGAAT CTCTCCAATG CTTGATTTTA ATTTTTAAAA 2280 AAGAGGAACA TATTACAAAG GAAGCAGAAT TTCAACATAA TCTTTAGATG GTAAATTATG 2340 TTTTACATTA GTCTGCATTA TTACCACAAT ACTTGCACCT GGCTGGTATG AGGAGTGTGT 2400 GTGTGGGTTA AAGGGAGCTG TTATTTACCT GCTTATCTAT CAGACTGGTA ATACCAATCT 2460 CACTCTGCAA ATTTAACATC AGGGATTTAC TGTTCATAAT AGAATAAATG CATATTGAGA 2520 ACCACACTTG AACTTAGCCC TTCTGACAGG AAACTTTCAA AGTTAGAAGT TACACTGAGC 2580 TTGAATTTTA AGAGAGAGGA AAAGTCATTT AATAAAACTA AAAAATGAAG GATGGATGGA 2640 TGGATGGATG CATAGGTAGA TGGATGGATG CATAAGTGGA TGGATGGATG GATGGGTGAA 2700 TGGATGGATG GATGGATGGA TGGATGGATG GATGGATGGA TGCATGGATG GATGGATGGA 2760 TGGATGGATG CATGGATGGA TGGATGGATG GATGCATGGA TGTATAGGTA TATGGATGGA 2820 TGGACAGATG GATGGATGGA TGCATAGGTA GATGGATGGA TGGATAAATG GATTGATGGA 2880 TGGATGGATG GATGGATGGA TAAATGGATG TATGGCTAAA TGGATAGATG GATAGATGCA 2940 TAGGTGGATG GATGGATCGA TGGGTAAATG 2970
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