Tag | Content |
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EnhancerAtlas ID | HS182-01750 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:204070640-204074570 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr1:204073699-204073713 | ATTCCCCTGGGACT | - | 6.33 | EBF1 | MA0154.3 | chr1:204073699-204073713 | ATTCCCCTGGGACT | + | 7.17 | FOSL2 | MA0478.1 | chr1:204073903-204073914 | CTGAGTCACCC | - | 6.02 | IRF1 | MA0050.2 | chr1:204071935-204071956 | ATAGAGAAACTGAAACTTCCC | - | 6.17 | IRF9 | MA0653.1 | chr1:204071937-204071952 | AGAGAAACTGAAACT | + | 6.28 | JUNB | MA0490.1 | chr1:204073903-204073914 | CTGAGTCACCC | - | 6.02 | KLF4 | MA0039.3 | chr1:204073569-204073580 | GCAGGGTGTGG | - | 6.62 | STAT1 | MA0137.3 | chr1:204070704-204070715 | TTTCCTGGAAA | - | 6.62 | ZNF263 | MA0528.1 | chr1:204071742-204071763 | GGAGCAGATGGAGGAGGAAGA | + | 6.48 | ZNF263 | MA0528.1 | chr1:204071751-204071772 | GGAGGAGGAAGAGGGTGGCGG | + | 6.66 | ZNF263 | MA0528.1 | chr1:204071748-204071769 | GATGGAGGAGGAAGAGGGTGG | + | 6.71 |
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| Number of super-enhancer constituents: 16 | ID | Coordinate | Tissue/cell |
SE_01182 | chr1:204071129-204074607 | Adrenal_Gland | SE_06365 | chr1:204070800-204074466 | Brain_Hippocampus_Middle | SE_24644 | chr1:204072637-204073956 | Colon_Crypt_2 | SE_29514 | chr1:204070868-204072610 | Fetal_Intestine_Large | SE_31799 | chr1:204070890-204072352 | Gastric | SE_31799 | chr1:204072461-204074581 | Gastric | SE_34793 | chr1:204069193-204075827 | HeLa | SE_42361 | chr1:204069421-204075729 | Lung | SE_47675 | chr1:204073025-204073996 | Pancreas | SE_49400 | chr1:204070904-204074543 | Right_Atrium | SE_50648 | chr1:204070818-204074547 | Sigmoid_Colon | SE_53078 | chr1:204070806-204074527 | Small_Intestine | SE_54451 | chr1:204071112-204074613 | Spleen | SE_65332 | chr1:204070923-204074836 | Pancreatic_islets | SE_68685 | chr1:204070894-204072274 | H9 | SE_68685 | chr1:204072447-204074590 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 204071387 | 204071653 | chr1 | 204073791 | 204074252 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I204100 | chr1 | 204069922 | 204075641 |
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Enhancer Sequence | AAAAAAGTGG CAGGAGGCCT TGGAAACATA CTGGTTTGGG GCTGAGTGGT CTGGCTGGTA 60 GAGGTTTCCT GGAAACACAG TCCTTCATTC AGCCACCACA ATACTAAGTG CCAATCTGCT 120 TTGTGCCAGG CATTGGGCTA AGTATTTTCT ATATAATAAC TTATCAGTTC TCTAGCAAGC 180 ATAAGAGGTA GGTATTGTTA GCCCCCATTT CAGACAATGA ATCTGAGGTG TAAAGAGGTT 240 AAGTCTCAAG TATTCACTGG GCTACCTAGA GCCCAGCTGC TTCCCAATTT TCCACCCTTC 300 ACCTCCTAAT CTAGATGACA ATGGTAAAAT GCCCATTACA GTTGTTCATC ACGGCTGTGT 360 GCCAGGCACT GGGCTTTGCC TGTGTTATCT CGTTTACTCT TTGAAACCCC ACTAGTGAGT 420 ATATATTACT ATTTGCCCCA GTTACAGATA AAGGCAGGAG GGTCATTTGA GCCCAGGAGT 480 TCAGGACCAG CCTGGGCAAC ATGGTGAGGC TGAGAGAGTT AAACTAGTTG GCTAGTTAAG 540 ACGGATGCTG GGTTTGAACC AATGCTGCGT GTCTCCCAGA GCCTCATTTC ACCATGTACT 600 ATGAGGGCTT AGTCTACATG GCTTAGACTT GTCACAAAGC AAAAGCCGAT AATGCCCAGC 660 CCACCCCAGT ACTGGGAGAA GGAGTGTTTG GCAAAGGTGA GATTTCATCA GCCTGGCGGG 720 TAAACATGGC TGTTTGCAGA CTAGTTGCGC TTGTCCTTTC CGCTGTCTGT AGTCATCCCT 780 ATGGTCCCCA CCTTCCTCTC CCTCTGGGGT TGGCAGGAGA ACGCAAGGGT TAATGATATA 840 GCACTTCACC CTTGTGGGCT CCAGAGGAAA TGAGGGAGCT CATGAGTTCT GCAGAGCTTT 900 TGTGTCATCA GCCGGGGAAG GGAAGGCACC GTGGCTTGGC CAGATAAGCG GTGGCGCTGC 960 GAATGTGGGG CTTCCTTGGC AGATTTGTAG CCTTTCCGCC TGTTTGCACT GTGGGGCACC 1020 TGCTGGGGCT TCCAGGGTGG TTGGGGACAT CAACAGGGCA TTCAGAAAAC TGATAACCTA 1080 GGCTAGGGAG GGAGACCTAC ATGGAGCAGA TGGAGGAGGA AGAGGGTGGC GGGCCCTGGT 1140 GTTCTGCAGG TGCATGTCTT CTGCTTGTTT GACCATGTGG GGGAAGGGGG TGGCGGTGGG 1200 TCAGGGAGCA AACATTTTTT TGATTTTCAC AAACACCATC ATATTCAGTC TTCTCTATCT 1260 CTATGGGGTA GGTGTTATTT GTTCCCATTT TAGAGATAGA GAAACTGAAA CTTCCCCATG 1320 GCCACACATC TAGTGGTATA TAATAGAGCC AGTCTTCAGA CACAGGTCCA TGTGACAAAG 1380 TCCTTTTTCC ATTAGCCACA CCAGGATGCC TCCCAGCAAT GCTGGGTCAT CACACCCACC 1440 CACCTGCCTC CGGAAGAGCT GGGCTGGCTG GGGAGGAGAA TAGGGTGTGA GTCCTTCTCC 1500 CCCTTGCCCT GGGGGCAGGG AGGGAGAGGG ACTCCTTCCT GCTTTAGGGC TCTTTCTCCT 1560 TACCTCCTTC CCTGAACATA TATTCTGTAC CAGATTCTGT AATTATACCT TATCTCTTAC 1620 TCACAAAATA GTTCTTGGAA TCTCTATTTT ACACATGAAG AAATGGGGGT TTTGAGAGGT 1680 GAAGTCTTTC CCCCAACTTG CCAGAGCTGC CTGGGTTTCT TTTGACTAAG TTTTCCTTGG 1740 CTATGACTCA AGTCAGAAAC AACTGCAATC CTGTAAGAGG TGAAGACAGT GGCCATTCTA 1800 TCTCTGCTGG ACCAGAGCCT GTTATTTTGC ACCGAGGAGA GTGGCCAGGG CATCAGCTGA 1860 TAAATGAAAG GATGTGGATT TAGACATCAG CGAGGCCTGA GTTCAAATGC TACTTCTGCT 1920 GGGCCCTCAG TAGGACGTTC TAGCCCCCGA GCCTTAGTCT TTGTAGTGTT CTTGTGAGGA 1980 TTAAGCAGGA ATGTGAATGA AGAGCCTTTC ACTTAGTGCT TGCAGCCAAG TAAGTGCTGT 2040 AGCATTGCAT GCTTGCTTTT TGCCTCCCAT TCCTTTGGTC AGTATTCAGG GCTATCCCCC 2100 AAGGGGCCTT TGACATGGCC AGTCAGCCTC AGCTGCACAA TTTCTGCATC TCCCAGCCCT 2160 AGGCTGGGCA CTGTCCCTGC AGGAAGCCAG ATGTGCTCAC CTGTCCAGGA CACAGGCTTG 2220 GCCTTGCCAT TGGGAAACAA GGATGAGGCC TACCCCTGCC TTCTAGCACT GTTGGGGTGC 2280 AGGAGAACCT GGAGACAGGC TTGGGTTCTA GAGGCAGGAA GGCCTCCAGA GAAGGGCCTC 2340 CTAGAGACAC TGTTGACCTC TTCTCGGTTT GGGACCTTCT GGAGGCACAC ATCACACTGG 2400 GAGCCTCAAT GGCGCTTTCA AGCAGTCCCA TCTGTCTCTT TCTCGACCCA CTCACTGGGT 2460 TGGGAGAAGA CTCAGGTGCC TCTGAGGCCT GAGGACCAGG TGGGAACATC ACAGCTACAG 2520 TCTCTCCCTG GCCACTGTTT TCCTTTGTGC CCTTGGGCCA GGGTCAGCTG AGTCCCGGCA 2580 GCCACAGAAG CTCAGGCTGG ACTGTGATTC TGTACCTGAG GTGCTGTGGG GAAGTGCCTC 2640 TTCTCCCATG CTTGGGAGTT GACCCAGCCT CTGTCTGATG TTGGCCACTC TACCAGGTGA 2700 ATGCCACCCT GACCAGCCTG GAAACAGCCG AGGGAGTGTT GGCTGTGGCC CCCCTGAGCT 2760 GGGCTAGACC AGACCGGCCG TGCCCTGGAT CTGATACCCC CCAGGGCTCA CAGAGGCTGG 2820 AAAGGGTGAG AGGGACTCGC AGGAAAGCTT TGTCCCAAGC CTGCAGCCAG TCCAGCTCCC 2880 AGCTCTGAGT AAACATTAGA GATAGGATCG GGTGTAGCCA GGAAGGGTGG CAGGGTGTGG 2940 TCTGTGAGAA GAATGGCAGG ATGTGGCACC GGGGCACTGT TCTGGGCACC CACGCCTTGG 3000 CCTATTGTTT AGGGCAGCCT GAGGTTCTCA GCTCTCTGGG GGCTTTCAGA GGAAGTGGCA 3060 TTCCCCTGGG ACTCAAGCCC TGCCCCACCC CTGCTGCATG GATCTCTTTC CCTGGTGATG 3120 CCCCTTGGCA CCACCCACTC AGAGCAAGCT TGGGAGTGGG AGCCAGCAGT GGAGGGGGAT 3180 TAGTGTGTGC CCAGCGGGGA AGTGTAGCCA TTGGCCCTCT CAGAGGGTCT GCCTGTCTGT 3240 TCAGGCTTCC TGTACCCCAG GGTCTGAGTC ACCCGTCATG CTACGATGAC TGGAATTTAT 3300 CTCTATCTTT ATCTTCATCT AGATATTTTT TGTAGGGTGG GGGAAGGCTG TCGTTGTGGA 3360 GGGAGGAAGG ACTGACAGTA AAAACTCCTT TGATTCCAAT CCAACAGGGT CAGTTGTTGA 3420 CTGGTTAGAA GAGGAAGTGG CTGGTGATTT GTTTTGGGCA GAAAGGGGCT AGGTTTGTGT 3480 GCGCCTGTGG GTTGGTGGGG TTCAGAGGGG CCGTGACAGG GCTGGTTGTG GGGAGGAGAG 3540 AGGAAGAGGA TCGGCACCTG CAGCGGGCTT TGTCATATAA GCGCCATGCT TTGAGCCACT 3600 GTCCCTCCAT GGAGGCGGGT GCCTCTCTAT ACCTTGTCTC AGGTGCTGGA TTTGGGGGCC 3660 TCGGGGCCTG GTAGGCACAA GCTGAGACTC AAGGCTCTGC ATGTCAAGGG CGAAGATGGC 3720 TGGAGCCCTC TCCTTAGAGG TCTTCACTTC TTAAGGATGC TCACTTGGGT GAGATAAGAC 3780 CACAGAGGAA GAAGAATGGA AGAGGGATTG TGAGGTGGGT TCCTGAGAAG GAAGGGAGGG 3840 CAGAGCAGAG ATGCCGCTTA GCGCCCCAGC TGGCTGAAGG CCTCTGACTC TGTATAATCT 3900 CTTTTTTTTT TGAGACAGAG TCTCCCTCAG 3930
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