Tag | Content |
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EnhancerAtlas ID | HS118-05054 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr12:124491500-124493400 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr12:124492374-124492395 | TTTTACTTTCCCTTTTTTTGT | + | 6.25 | MNX1 | MA0707.1 | chr12:124493139-124493149 | TTTAATTACC | - | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_00523 | chr12:124491995-124493658 | Adipose_Nuclei | SE_39595 | chr12:124490097-124493548 | Jurkat | SE_66717 | chr12:124490097-124493548 | Jurkat |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 3 | ID | Chromosome | Start | End |
GH12I124005 | chr12 | 124490404 | 124492111 | GH12I124007 | chr12 | 124492393 | 124492790 | GH12I124008 | chr12 | 124492841 | 124492990 |
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Enhancer Sequence | CTGTGAGCTC TGTGGGGTTC CATAACCTGT ATCTGCCTCT GGATTTACAG CTGCCTCTAT 60 CTGTGTGGAA GAGTTGGGTG GGGGCTGTGT TAGGCGAGTC TGTACTGGAG ATCCTTGCTG 120 TGTGTTGGCC TTTCTGTTCT TTGGTTGGTC ACGTGGAAAA TTTGCCGGAG TTTCTTTTAT 180 CTTTCTTTTT CCTACAGAAT GCACCTTAAC CCCTCTCATC CCCCCACCGT GCAGTGAGAC 240 TTACAGACAG GTCTGAGAAT TTTATCTGGA AGGAATGGCA GTGCCTGATG CCTGAAGAAG 300 AACTCTAGTG GGAGGTCATG TTGGACTCCC CTGTCAGGGA CCTTGGTATT GAACTGTTGC 360 CCTTCTGAGC AGAGTTGGAC TCTCCTGAGG CTAGGCTGGC GGAGTACCCT AACCCTGGCA 420 GCTTGATTCC TGGAGGGGGC TCTGGAAGAC ACCCCTGCTG GGGTTAGCTT GCCAGGCAAA 480 AGAGCAGAGC GCAGTGCTGC TGCCTTTGTC TTTTGCTTGT CGCTGCCCTG CAGCCACTGC 540 CTTCGCCTGC AGCCACTGCC TTTGCCTGCT GTCCAGAGGC CTCTTCCTGT GTTCATTCTC 600 CTGTGCTCAG GATTGACTGG GGAAATGAGA GCCGTTTCGG GGATTATATT CGTTTCAGTC 660 ACAGTTGCCC CTCTATGCGG TGGTCCTGGG ATTAGTTTGC CATTGCCAGA AGAGCAGGAA 720 AGGAATATCT TAGCATTCAC AGATTTTTTT TTTTAACCAT GAAAATTTCA ACCATACACA 780 ATATTTTACA ATAGAATCTT TTAGAGTAGA CTATTATCTC TTACCTAAAT GCAATGGTTA 840 CAATGATTTT ACCACATTTG CTTTGTCTGC TCTTTTTTAC TTTCCCTTTT TTTGTTTGTT 900 TGCTGAAGCA TTTTAAGTCA CACATGTCAG ACGACATGTC CCGTCATTCC TGTTCTTCAC 960 TGTGCATCTC TAAGGCTGTA GACATTGGTT TACATAGCTA CAATGACATG ATCACATAGT 1020 TAACAGCACA CAGTGTAATC TCATACCCCG AATCACATTT CCTTGACTGT CCTCTTTTAG 1080 CAGCTGGTTT GCTTCAGATT GCAAAGAAGT TCCTCTGATT ACATCTGATT GTTATGTCTC 1140 AAATCGCTTT CATTTAGAGC AACTCCTCCC ACCTTACCGG CTTTTTTTCC CTCGTGTCCT 1200 TATTGCAAAA AAAAAGGGGC AGTTGTGCTG TAGAGTGGCT CACCTTTTGA TATTTTGCTA 1260 CTTGCTTCCT AGTAGTTCCT CTGTCCCTTC AGTTCTTTCC ATTAAAAATT AGCTCCAGAG 1320 GCTTGATTAG GTTTTGCTTC AGTCTTTTGA CAAGAATGTC TTCAGAGGGT GCTGGGTGTT 1380 TCCCATTGCA CCACAGCAGG AGGCACACGT GTCTGGTTGT TCCTCTTTGA GTCATGCTAA 1440 GATCGATCCC TGGCTTCAGG TGGTGACAGC CTGGTCCTGG CAGTGTCAAG TCCTGGATCA 1500 GCCTTCCAGC CGCTTTTTTC ACCCATTGCT TTTCATGGTT TGAATCAGGT GTTTGATGAG 1560 GAGAATGCAC ATATTAGCTG GTTGTTTCTT TGTCTTGAAA GAGAGTTCAT AGAGGAAATA 1620 GGATAGATGC TTCTCTCCAT TTAATTACCA ATTTTTAGGG TAAAAAGTTG GGCCCCTAGT 1680 TAATTCCAAT TTTGTTCAGT GCCTTGGGTC TCTCCATCTC TCTGCCTGCC TGTCTGTCTC 1740 TTTCTTCCCC ATTCTCTACA GTCATTATGA GCTCCTGGGG TTTGTATATT GAATGCGTCT 1800 CACTCAATTG CCTTTCTTAT TCCTTTTGAT GCTCAGTTGC ATGATTGGCT CTGTGTTCCT 1860 TTGGCACGGC CCTCTTGCTT TCTGGCATAA CAGGATGTCC 1900
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