Tag | Content |
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EnhancerAtlas ID | HS146-08379 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr2:86262750-86265820 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr2:86265787-86265798 | TCAAGGTCAAT | + | 6.02 | EWSR1-FLI1 | MA0149.1 | chr2:86263650-86263668 | GGATGGGAGAAAGGAAGG | + | 6.64 | EWSR1-FLI1 | MA0149.1 | chr2:86263627-86263645 | GGCAGAGAGGAAGGAAGG | + | 7.01 | STAT1 | MA0137.3 | chr2:86264202-86264213 | TTTCCCAGAAA | - | 6.02 | STAT3 | MA0144.2 | chr2:86264202-86264213 | TTTCCCAGAAA | - | 6.32 | Stat4 | MA0518.1 | chr2:86264199-86264213 | CCATTTCCCAGAAA | - | 6.98 | ZNF263 | MA0528.1 | chr2:86263636-86263657 | GAAGGAAGGGGGAGGGATGGG | + | 6.01 | ZNF263 | MA0528.1 | chr2:86263647-86263668 | GAGGGATGGGAGAAAGGAAGG | + | 6.03 | ZNF263 | MA0528.1 | chr2:86263632-86263653 | AGAGGAAGGAAGGGGGAGGGA | + | 6.26 | ZNF263 | MA0528.1 | chr2:86263643-86263664 | GGGGGAGGGATGGGAGAAAGG | + | 7.1 |
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| Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
SE_03813 | chr2:86262297-86266166 | Brain_Angular_Gyrus | SE_05613 | chr2:86260895-86267611 | Brain_Cingulate_Gyrus | SE_06560 | chr2:86259849-86268929 | Brain_Hippocampus_Middle | SE_08740 | chr2:86260188-86267713 | Brain_Inferior_Temporal_Lobe | SE_09559 | chr2:86261844-86267074 | CD14 | SE_11334 | chr2:86259221-86269184 | CD20 | SE_12313 | chr2:86260837-86267698 | CD3 | SE_16209 | chr2:86262330-86268477 | CD4_Naive_Primary_7pool | SE_16726 | chr2:86261964-86266929 | CD4_Naive_Primary_8pool | SE_17752 | chr2:86258671-86270087 | CD4p_CD25-_CD45RAp_Naive | SE_20703 | chr2:86260976-86267295 | CD56 | SE_30867 | chr2:86262173-86266133 | Fetal_Muscle | SE_30916 | chr2:86260730-86269877 | Fetal_Thymus | SE_44100 | chr2:86261220-86268112 | MM1S | SE_55256 | chr2:86262205-86269136 | Thymus | SE_65948 | chr2:86258740-86269074 | Pancreatic_islets | SE_67122 | chr2:86259454-86266781 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 86262986 | 86263343 | chr2 | 86262800 | 86265600 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I086032 | chr2 | 86260026 | 86269508 |
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Enhancer Sequence | CATCTGGCCT CAACTCTAAC TGCCCATCTG CTCCCTCCAC CCTGTGCACC CTTTGGGCCT 60 TTGCTTGAGC GGCTCACTCT GCCAGTAACT TCCCTGGCCA ATATCTACCT ACTGAAGCTG 120 TACTCATCCT TCAAGGCCAG GCCTCAGCAG CTGTAACTCC TCCAAGAAGC CCTCCCTGAT 180 TCCCCCAGTT GGGGATGCCT TCTGCCTTCC CTGCCTCTTT TGGTGACCAG GACTTGTGGA 240 GAACGTAGGA GGGAAGGAGG TGAGAAGGCA GAATGAATGG CTGGTGAGTA AGTGGTAGGC 300 ATGTGACCAG TGTGCCAGTT TTCCTGGAGG TGCAATTTGC CCTTCTATGG TTTTGCCAAG 360 AGCAGGGGAA CTAACGGCCC ACAGTGACTG CCTTCTCAAG GTTGTGCAGC TCACCTGAAT 420 GTAGCAACAG AAAGGGAACA GGAGGGGCAG GGGCAGAGAA GCCTCCCGTC CCACGTAAAT 480 AATTACAAAC AGAGCACATG ACCCCTGGCG GTTTCTGAAC GCGCCTGGCA ACAGCTCCAC 540 CACCTGCTGT TTGGAAAGTC AGATTCACAG AAGCTACAAT TACAGACTGT CAGCTGGGTC 600 TTTTCATGGC TGGGGACCGG AGGCCAAAAC TTACAGCCCC TAACTCCTAG CTCAGTGCTC 660 TTTCCACTTC ATCTCCCCTG CCACCTGCCA GACAATTTAC ACAAACAGCC CATGTGATGG 720 GTGCCAGTGC AGAGATCTGG GGGGCCTTCT ACGCTTGTAT ATCTCTACCT AGGGAACCAT 780 CTGTCTCGTG CTGTTTTTCT CCAGGCTCTG TCAAGGGTCT CATGACTCCA CAGCTGGGAG 840 AAGGGAGGGT GGGGGCAAAG AGAAAGAAAA AGAGGGTGGC AGAGAGGAAG GAAGGGGGAG 900 GGATGGGAGA AAGGAAGGAG AAAAAGCTTC TTGGGGGTTG GCTGCTCTTT TGAAAGTGCA 960 CTCACACTTC CTCCCATTTC CTGTGGGCGG CCAGAGGCCT GAACACAGCT GCTCTGCTGC 1020 CTGGGGCCTG ACAAAGGGAG TCCAGACCGC ACCCAGCTCA TCCACTGCCC CATCTTTTAG 1080 CTCTGCCTAA CCCCTCAGCC CCATTCTGCT GAGTCCTTGA GGCCACCTCC ACCAAAAGCT 1140 ACTGCGCATG GCTTTATTTA TCACAGATTT TCAAGTTCAC AAGCAAAACA CAGGGAGGAG 1200 TTGAAAAAGT ACTTCACGGC TGGGAACAAG CCAGGGCTGT CCCTCATCAG GAAGAAGTCT 1260 TAAAAAGTGA TTTCCTATTT TCAATTCCAT GAGGTAATAT AAGTAAAAAG AACCCCAGCA 1320 TGGGCTGGCG CCAGCCTCAT GCCGACCTAC CTGCTGGGCT GGCCTGGGCC TCCTGTGAAC 1380 AGAACTGGGG CAAAACATCT AACTCCGTCC ACCCTTAGTT ATTCTCTAGA GGCCATGAAA 1440 TCTGAATTCC CATTTCCCAG AAAACCACTG CCAGGCCAGC ACAAACGCCC CCTGCACTTG 1500 GTAGTTATGT TCCTCGCTGT TAATTAAGGA GCTGGCAGGC GGGTGCACAC AGCACTCCCC 1560 TGCCACTCTG CCCAGTGCCC AGATAGCACA GAGGACCACT CGACAGAAGG AATGTTCTCA 1620 GCCCAGGCTG GCACCAACGC AGGTGCTCCT GAGGCCCAGC CAACAACAAC TTCACCCAGG 1680 GCTCGTGAAC TGGGGCAGGA AGCACCTGGC CAGTGACCCC CGTCCAAAGG ACTGAGTTCA 1740 CATCCAAGCT CCTCCACCCC AAGACCCACC ATCCCAAATG CCACCTGCAC AGAGGGCTGG 1800 CTCGAGGCCA GGCCCCATAA GGTGAGAGGG CAGAGGGCTG AGGGCAGAAA AGTCGTACTG 1860 TGTTGCCCAC GCCTGCCCCC GTGACTCAGC GACGAATGGG CATGGCTCAG TATGTGTTTG 1920 TGGGATGGCT GAGTGCAGGG AGCTTTCTGC TTCTGCTCTG TCATTGCTTC TCTATCTGAG 1980 CAGCTCCCAG AAGACCAAGA ACTGGTCTAG ATTAGAGGCA GTGGTCAGTG GCCTGTGGCC 2040 AGATCCTGCA ACAGATGAGA ACCATCTGGG CCTTACTGGG CTTTTAAAAA CACATGAATT 2100 AGTTGCTGAT GTTTAAAAGT CAGGAGACCT CAATTATATA AAAGCAAAGG CAAGTAAACA 2160 AGTGACCCAA GAAAGAAAAA AACGTAGGGG GTGGGAAGCT TGTTTTCTTT CTTTTTAAAT 2220 CAAAAGATGT GGCCCCCCGG GCCTCCATTC CTGCATAGTA ACAGGTGCCC CTTGAGACAG 2280 GTTCCACACT CTTCAGTCTG CCGGGGGCCT CCAAGCCTGC TTCACTGGCC TGTCACCTGC 2340 TGGGCTATGC AGCCTTTTTG TGTTCACACT TCACCGTCTA GGGTTAGCTG GTGAGTCAAA 2400 AATGCTTCGT GGGCTCTTCC AGTCTTGCCC CAGTCCCCAA AAAGCCCATC CTCCTGCTCC 2460 CCGGAACTCA GCATTGTGGC CTCTGCTTTT CAAATATCTA ACAGTAACTT GAACTTGAGA 2520 CAAAAGTTCC TTTTCCCTAC TGGACAGGAA CTCGGGACAG GAACTCGAAT TTCTCTGGAG 2580 GCAATCCTGG TTATAGAATG GAGATCTAAC AGCAGCGTGC CACCCGCACA TTGTTCATTA 2640 TTCACAGAAT CTAAATGCAT CAGGAACCAC ATTATACTGC CTGCAGTAAC ACCCTAGCAA 2700 ACATTAACAG CATGTGCTGC TCCGACACCA CAGAAGCACC GCTTTGATGG TGCTCCCTTC 2760 TCTTTACCAC ACCCACATTT CCATGTCTTA ATGCCTGCAA GCCCCAGAAG ACAACAATCC 2820 TGACGTCAAC CCAAGAGAAG AAATGGGCTC AGGGAGTGAC GTGTGGCTAA GAAAGTCATA 2880 CCCACAAGCC AGACTGTGGT CAGGTTTCCA GATCAGGCTG CAAGGCCCTC TGCTTCCTAA 2940 ACACTTCCCT TGAAGGGCTC ATTTGGGCAA AGGCACTCAA TCTCTAGGAG CCTTGTGGCT 3000 AGGTGCTTCC TGCCCCAGTT CAAGCGCATT CTCTGGGTCA AGGTCAATGA CAATCACAGC 3060 CTGAGCCCTG 3070
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