Tag | Content |
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EnhancerAtlas ID | HS073-07762 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr19:44255570-44258800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr19:44257542-44257554 | TTCTGTTTACTG | - | 6.02 | JUN(var.2) | MA0489.1 | chr19:44257365-44257379 | GGAAAATGACTCAT | + | 6.76 | KLF16 | MA0741.1 | chr19:44258732-44258743 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr19:44258733-44258743 | GGGGCGGGGC | - | 6.02 | SP1 | MA0079.4 | chr19:44258731-44258746 | CGGGGGCGGGGCCTG | - | 6.11 | SP4 | MA0685.1 | chr19:44258729-44258746 | GGCGGGGGCGGGGCCTG | - | 6.26 | Zfx | MA0146.2 | chr19:44258732-44258746 | GGGGGCGGGGCCTG | + | 6.19 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_02767 | chr19:44256100-44260167 | Astrocytes | SE_09619 | chr19:44255368-44262466 | CD14 | SE_10575 | chr19:44256833-44260060 | CD19_Primary | SE_11483 | chr19:44255253-44262275 | CD20 | SE_13735 | chr19:44255931-44257680 | CD34_Primary_RO01536 | SE_13735 | chr19:44257681-44261073 | CD34_Primary_RO01536 | SE_14657 | chr19:44256014-44261046 | CD4_Memory_Primary_7pool | SE_18182 | chr19:44255605-44260321 | CD4p_CD25-_CD45ROp_Memory | SE_18680 | chr19:44255276-44260362 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19217 | chr19:44256242-44260273 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20985 | chr19:44256876-44261109 | CD8_Memory_7pool | SE_23510 | chr19:44257834-44261164 | Colon_Crypt_1 | SE_23897 | chr19:44258182-44260089 | Colon_Crypt_2 | SE_27247 | chr19:44256975-44262719 | Esophagus | SE_31804 | chr19:44257590-44260338 | Gastric | SE_32542 | chr19:44255365-44264271 | GM12878 | SE_33868 | chr19:44256868-44261203 | HCC1954 | SE_34298 | chr19:44255426-44256716 | HCT-116 | SE_34298 | chr19:44256799-44272203 | HCT-116 | SE_34813 | chr19:44256968-44262677 | HeLa | SE_36558 | chr19:44255760-44264581 | HMEC | SE_37675 | chr19:44254852-44262981 | HSMMtube | SE_39921 | chr19:44256960-44261248 | K562 | SE_50403 | chr19:44256946-44260066 | Sigmoid_Colon | SE_53073 | chr19:44256976-44257621 | Small_Intestine | SE_53073 | chr19:44257665-44260035 | Small_Intestine | SE_53761 | chr19:44256508-44260208 | Spleen | SE_56117 | chr19:44257406-44262941 | u87 | SE_59025 | chr19:44248893-44290143 | Ly3 | SE_60730 | chr19:44257018-44289948 | DHL6 | SE_62525 | chr19:44242576-44303622 | Tonsil | SE_64692 | chr19:44256932-44264220 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 44255843 | 44256372 | chr19 | 44256380 | 44256453 |
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Enhancer Sequence | GAGCCACCAT GCCCGGCCAA GGCCCTTCCT TTCAACAGAG CTCTGGGCCT GTGGTAGCAA 60 CTGCAAGCTG GTTCCCAACA TCCACTCCTG ACTTCTTCCA AAAAAGTAAA ACCCTCAGTT 120 CTGAGCTAGG TACATGGCTA TCCAGAACAA ACTTCTCATC CTTGTTTGCA GTTAGGTGTG 180 GCCATGTGAG TAAGTACTTT CTGGCTATGG TATGACACTA GAAGTGTGGC TTGGCAGCTT 240 CCAGAAACTT CCCTTCACAG ACTCTGGCAC ATGCCTTCTG CCCCTTCCTC CCAGTGACAG 300 GAATGTGGGT GTGGAGGTTG GAGCTCAAGC AGCTATCCTG GGCTGTAAGG CAATTTAATG 360 GAAGGTACAA TAAAACAAGA CACAAGGTTG GGGGGTTCCA CGTTAACCTT GAATTGCCTA 420 CTTCGAGAGG CAGTGAAAAA CAAATACACA TCTATCTCTT ACTTGCAGCC AAAACTATTC 480 CCAACTATTA AAATGCTCCA ACATAAATAA ACTCACAGGG GCAAGTTCAC ATAAAAATAG 540 GATATTCTCC TTACCAAAAT GCAGCAAGGC ATTTGCTTAC AAACCAGCAA TGTGATCCTC 600 AGTCCAACAG CTACTCTTGA TTAGTCATTA CTAGTGTATG TCATGGTGGG GCTCCAGCCA 660 CTTACTAGTG TATGTCATGG TGAGGTTCCA ACACTCAAGG GCCTATTTTC ACCTGGTATC 720 CCACTACATT TCAGTGTCTG TCTGTCTTCC GTTCCTGACG GTCTGCCTTC CCTCACAGTG 780 AATTTCATTT CAAGGTGTCT CCAGTGTTTA TTCTATTTGA GATGTTATAT AATGTCTGGC 840 TACCTATGCA ACCCACTCTC CACCATTTCA GTATCTGTTT ACAGGTCCTT AGAGAGTTTT 900 CCCAGCTGTT CACACATCAG TCTAGGGTGG TATTTGACTA CTTAACTGTT TGTAGAACTC 960 AGTGGGGCTA TCTGCTCAAG CTCAGAAGTC AGGTTGACAA AGTGTGGCCT AGGGGCCAAA 1020 TCTGGTCTGC TTTCTGTTTT TGTAAATAGA AAGTTTTATC GGAACATGGC CACATCCATC 1080 AATTTAGAAA CTGTCTGTGG CTGCCTTCTT GATGCAATGG CAGAGCTGAG ACAGACAATA 1140 CAGTCTGCAG GGCCTAAAAT AATTATTCTC TGGCCTTAAC AGAAAGTTTT ACTGAATGGC 1200 CGAGTATGGT GGCTCACACC TGTAATCCCG ACACTTTGGG AGGCCGAGAC AGGAGGACTG 1260 CTTCAGCCCA GGAGTTCGAG ACCAGCTTGG GCAACATAGC AAGATCCTGT CTCTATATAA 1320 CATTTAAAAA AGAAAAAAGT AGCTGGGCGT GGTGACATGC ACCTGTAGTC CCAGCTACTT 1380 GGGAGGCTGA GGTGGTGGGA TCACTTGAGC CTGGGAGGTC AAGGCTGCCA TGATCATGCT 1440 GCACCACTGC ACTCTAGCCT GGGTAACAAA GCAAGACCCT GTCTAAAAAA AAAAAAAAGC 1500 AGAACCCTGT CTCAAAAAAA CAGTTTGCTG ACCCTTGCTT AGCTTGGAAG TATCTGTTAA 1560 ATCCCTCCAT GAATCCTCCC CTGCCCCACC TCATAATGAC ATAAACAGGT CCCTCCGAGA 1620 CTCTCCAGAA TGGAAGGGTC TGTTTACAAG ATGCAGTCAT AATTTTGCTA GCCAGACAAG 1680 TGGCTTGTCT AGCTCCTCTC CTACTGTGCT ACATGACCTC TCCCAGAGCC ACAAGCCAGG 1740 CTGAAGACTG CTTTCCTAGA CAGAGGAGGA CAAGGGCCTG TTTACAGCTG CTTAGGGAAA 1800 ATGACTCATT CCATACCGAA ATGACTGCTT AGTCTGGGAT GGAGATTCTC CCCAGAATCT 1860 GAGACTCCTC CCTCACTTGC AATTAAGTGT CTTTACACAT TATTCTGAAA TCTACCCAGT 1920 GCTTAAGTAC TTGTCTTCAT GCCTCAATTG GGATACTGCC CAGCCCTGAG GTTTCTGTTT 1980 ACTGGCCTAT GAGGATGCCC TTTCCTGTGC AAAGTAAGCG CCCCTGTGTG AATGCTTTTC 2040 TTTTTTTTTT TTTTTTTTTT TTGAGACGGT CTTGCTCTGT TGCCCAGGCT GGAGTGCAGT 2100 GGCACGATCT CAGCTGGCTG CGGCCTCTGC CTCCCGGGTT CAGGCAATTC TCCTGCCTCA 2160 GCCTCCCAAG TAGGTGGGAT TACAGGTGCA TACCACCAGG CCGGGCTAAG TTTTGCATTT 2220 TCAGTAGAGA CGGGGTTTCG CCATGTTGGC CAGGCTGGTA TCGAACTCCT GGCCTCAAGT 2280 GATTCGCCAG CCTCGGTCTC CCAAAGTGAT CGGATTCCCC GGGTAAGCCA CCGCACCTGG 2340 CCTCCCTGTG CCCTTTATTC TGGGAGCTTC CACAGTATCT GAATGTGGGG AGTTCCTTGG 2400 AACTTAAAAG CCCACCTAAA CCAGGTGTGG AGGATACAGT GAGCCGAGAT CGTGCCACTG 2460 CACTCCAGCC TGGGCGACAG AGCGAGACTC TTGTCTCAAA GAAAAAAAAA AAAAACCCCA 2520 CCCACATGCA AGCTGGGGAC TTCCAATGCT GTTTCCGGGC TCCTTTGGGG ATTACCCCCA 2580 AACTTAGGAA AGCTGGTCTA TTTAAGTGTC TGCTGATGGA CTTCTAGGGT GACTTCCCGA 2640 AAATTAACAA ATCGAATTTA CATATTTTTG GGGAGTGTCT CCTCAGTATT TAGGCATCGC 2700 TTCACACACT CCCTTCGGGG ATCTCCCAGA ACCTCACTAT TTGCAAATAT TTGGGGAGAC 2760 TCTCCCGATT CCTGAGTATG TAAGCCCACT TCGTGGGGCA CTCCCCAGCC CAGAACTGTA 2820 GTCGATTTGC ACATTTTCCT AAGGACTCCC TAGGATTTAA ACTTCTCTCT ACGGGGTTCT 2880 AGAAGGGAGC CTCCCCCGGA TTTAGGCATT GCTTTACAAA GCTTCCCTCG GGGAACCCAA 2940 CTCAAGTTTC TCGTTACACG TTATTGGGGC GGCCTCCCCA GTACTTGACG GGCAGTTTGC 3000 AGGCTGTACT TGGATCTCGC AGAGCATAAG TTTCTCATTT ACACGTTATT TCCGTCCCCC 3060 GCCCCCATTC CTGCCAACCC AGTATCGAAT TGACGGTCGC CGGCCCCCTA CTCAGTGCCG 3120 CACCCCCGCC GGACGTCCCA GCGACCTTTC AATGGCCAAG GCGGGGGCGG GGCCTGCCGG 3180 AGCGCCCCGC CCGCCGCCGG TGCGCTAGCC TCGCGCGGGC TCGCGGCCCC 3230
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