Tag | Content |
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EnhancerAtlas ID | HS133-16939 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:55337600-55340310 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr2:55339033-55339048 | CAGTATGACTCAGCG | + | 6.14 | SPI1 | MA0080.4 | chr2:55340037-55340051 | AAAAAGAGGAAGCA | + | 6.41 | SPIC | MA0687.1 | chr2:55340037-55340051 | AAAAAGAGGAAGCA | + | 6.59 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_00239 | chr2:55335449-55341307 | Adipose_Nuclei | SE_03190 | chr2:55338246-55341485 | Brain_Angular_Gyrus | SE_03921 | chr2:55337959-55342543 | Brain_Anterior_Caudate | SE_04845 | chr2:55334069-55343673 | Brain_Cingulate_Gyrus | SE_05873 | chr2:55336098-55342734 | Brain_Hippocampus_Middle | SE_06720 | chr2:55334097-55353338 | Brain_Hippocampus_Middle_150 | SE_07801 | chr2:55334319-55343521 | Brain_Inferior_Temporal_Lobe | SE_08941 | chr2:55338509-55339760 | Brain_Mid_Frontal_Lobe | SE_13769 | chr2:55337425-55341267 | CD34_Primary_RO01536 | SE_14856 | chr2:55337815-55341145 | CD4_Memory_Primary_7pool | SE_21142 | chr2:55337888-55341249 | CD8_Memory_7pool | SE_26467 | chr2:55337939-55341557 | Duodenum_Smooth_Muscle | SE_27564 | chr2:55338445-55341052 | Esophagus | SE_30501 | chr2:55338224-55341356 | Fetal_Muscle | SE_33603 | chr2:55333933-55341699 | H2171 | SE_37014 | chr2:55332846-55341638 | HSMMtube | SE_39299 | chr2:55338444-55341133 | IMR90 | SE_39897 | chr2:55338158-55341177 | K562 | SE_43033 | chr2:55338423-55341180 | Lung | SE_45296 | chr2:55337335-55337891 | NHLF | SE_45296 | chr2:55338190-55340827 | NHLF | SE_46551 | chr2:55336120-55341289 | Osteoblasts | SE_49902 | chr2:55338117-55341311 | RPMI-8402 | SE_51987 | chr2:55338261-55340673 | Skeletal_Muscle_Myoblast | SE_54907 | chr2:55334155-55341221 | Stomach_Smooth_Muscle | SE_56652 | chr2:55336443-55341447 | u87 | SE_63794 | chr2:55338223-55340673 | HSMM |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 55338983 | 55339153 | chr2 | 55338487 | 55338659 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I055106 | chr2 | 55333325 | 55341394 |
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Enhancer Sequence | AATATCAAAA CAAACAGAAC AATCAGGAAT ACCCTATGAC ATATCACAGC CAATAAAGGC 60 TCAAAAAATT CTTGCTGATG AAGAAAACAA ATGTTCCCAA ACAGCATTTC CTGGTTACTT 120 ATCAATAATG CAGACCAATG TCAATCTATC TGAGGGCGCA TATACGTCCA TTTGGATCCT 180 TTAAAAAAAA CTGTCTCATT CTTTAAATAA ATGTCAAGGG TGTTTACTCC AGAAATAAAA 240 TAGAAAGCCA ACCTCAAATC AGGAAAAATA CAGATTAAAA ATATATCTAC GCCAGGCCAG 300 GCACGGTAGC TCATGCCTAT AATCCCAGCA CTTTGGGAGG CCAAGGCAGG CAGGTCGCCT 360 GAGATCGGGA GTTCAAGACC AGCCTGGTCA ACATGGCAAA ACCCTGTCTC TACTAAAAAT 420 ACAAAAATTA GCTGGGCGTG GTGGCACATG CCTGTAATCC CAGCTACTTG GGAAGCTGAG 480 GCAGGAGAAT TGCTTGAACC CAGGAGGTGG AGGTTGCAGT GAGCCGAGAT CGTACCACGG 540 TACTCCAGCC GGGGCAACTG AGTAAGACTG TGTCTCAAAA TAACAATAAT AATAATAATA 600 ATGTATCTCC GCATGGGGGA TAAGGTCTGA AAAAAAGAAA AGAATAAAAA CAAAATAAAA 660 ACAAATTGTC TTTATTTTTA CTTGCTTGCT TGCTAACCTT GGGAAATTTG CTAGCTGCAA 720 AGTTGCTTTT TATTTTCCAA TAATTCTTGA GGGATCACTG GAATACTTGC ATGAAAAAAA 780 AAAATTCACT TTAACCTCAC TCTTCCGAGA TTTTAAAAAC AGAGCAAGCA CAGAGATAAC 840 AAAGAAACCT TTTTCAGAGG CACCCTCAAA TCTTAGGCCC AAATAGATGG TGGTATCAAC 900 AGAAACAACG AAATATCCAT AGCAACTGTG GAAAGCAGAT TCTCATCCCA TAGTGAGATA 960 ATAAATAAAG TCACTGCCTT TTGTGACACC TTACTCAACC TCAGACAGAA ATAAATGTTC 1020 CTCACTCCTG TTCGCATAAA TCCACCTAGC TAGTGTTTGT GGGAGCAGAG GGAGGATTGT 1080 TCCCCAATCC AGGCCCACGA AAGTGGCTTT GCCTTCCACA GCACCTCCCA CCCTCTGCTG 1140 GGAGTCACAG ACCTCTCCTA AGGACCCACT CAGGAGGGTG TTTGGGGCTG TTTAGGAGGA 1200 GGGGTCTCCA CTGGCTAGTT TGGAGGAAAT TCAACGAAAT CGAAGCCCAA CTGTAGGGGC 1260 CATGTACAGA GTAAGTGTTG AAAAAACGTT AATGTCCACC CTTCCTTTAT CCAGACACAT 1320 TGAACAGATA TTCACTGAAA TGTCCTTAAA AAATCTACCT CACCCCATGT CTATCCATCT 1380 TCCCGAATGC TGCCTGCCTC CTGCCTTGTG ACCAGCTCTG CCGGCAGACC CTGCAGTATG 1440 ACTCAGCGTG TTGAAATCCG CCTCTGTGGG CACGCACTGC TCTCAAAACT GCTTCAACCA 1500 CCAGAAGCAG TTAATTGCAA TGAGTCTCTG GGGATCCTGC TCCAATGGCG ACACTCAAGA 1560 GGAAGCAACC ACCTAGGCAA TACCTTCCTA TTAAATGCTA CCAAACTCCA GAAAGAGCGT 1620 GCCTTGGCTT TGTGAGGAGC TCAGAGGCTC TGAGAGGCCC CCTGTGGGGG AGCGTGTTCA 1680 GGACTATATG AGGCCTACCT TCCCAGCTCA CCTGCACTGG GCTGAGATGA TGGTGGTGAC 1740 AATGACAAAT AATACTAAGA AGAAAGGTAC CACTGACTGA ACACTTATCA TTTGCTAAGC 1800 ACTTGGCATA TGTTGCCTCA TCTACCCCCG GACAGCAACC CCGTAAAATC CTCATTTTAC 1860 AGGTGAGGAA ACCAGAGGTC ACAGAGCCAA AGTCAAGTGG TGATTAAGCA AGGCTTGAGC 1920 CCAGACTGTG GGGTTAGGGG TCTAGGCTCC CAACCACGTC AACACTACTG GCTTTAGAGC 1980 AGCTGCACTT TCCACACTAG TATTGTTCTA AATCTAAGCA CGGCCAGAGG AAAGAATAGG 2040 AAGCTCCACA CTGACCTCTA AGCTTTTTAT AGAGAAGCAT CTCCCCAGAC ACAGCCCCTC 2100 CAGCGAGCCT GGAGCCGGGC TGCCTCAGCT GTGTCTGCAG CAGTCCTCAG AGGCCCTGCT 2160 GGAACCTGAC CCTGAAGCTC CCAGCATCCA CGCTGCCGCT GGCTCCCAGC CCCGCCTTGC 2220 GGCTCGAGCA TAGCCATGAA CAGCTCTGAT GAATTATCTA CCAGAGGAGA ACTCCAATTG 2280 TATCATCAAA AGAGAGTTGG GGATTATCTG TTATTTTCAT TGTCCTTGCC ACTTCAGCCG 2340 CTATTTATTC AGAGCTGCTC ATGGCTCTGG CTTCCTTGTT TTATTTCTTC TGCCAACCCC 2400 CAGCTGGAGT TTCTGGAGCA ACCAAATAGC TAAAAACAAA AAGAGGAAGC AGCAACAGTC 2460 TGACATTTAC AAAGATGGAA AAATTGCTCT CTAGACACAT GACAACAAAC TGTAGAAAGA 2520 AAAATTGTGG CAAGATCAAC GTGAGCAACT GGGAGCTCAG TGGATGGTCC ATAGATAGAA 2580 GGCCCTGGCC ACACTGTGAT TCCAGGGCCC CAAAAACCAC CAGCACTGGT GTGAGAAGGA 2640 GGAAGACCGT GACCTGACAT TAAGAGAAAG GCTATGTCCT GTGCTGTTGC TAGAAAAATA 2700 AAAAGGCCAC 2710
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