Tag | Content |
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EnhancerAtlas ID | HS118-19368 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr9:99253620-99256020 |
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) |
STAT1 | MA0137.3 | chr9:99253808-99253819 | TTTCCTGGAAA | - | 6.62 | Stat4 | MA0518.1 | chr9:99253805-99253819 | CCCTTTCCTGGAAA | - | 7.64 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_06636 | chr9:99252833-99257356 | Brain_Hippocampus_Middle | SE_08722 | chr9:99255003-99257268 | Brain_Inferior_Temporal_Lobe | SE_35526 | chr9:99251238-99256493 | HepG2 | SE_44436 | chr9:99253021-99254729 | NHDF-Ad |
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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: 1 | ID | Chromosome | Start | End |
GH09I096490 | chr9 | 99253072 | 99255508 |
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Enhancer Sequence | TTGTGTAGAG AAAACAGTCC TTTGGTTACT CCAGGCCACA GCAGTCGGTC ATGATTTTGT 60 TGAATAATCA AAGTTGAATC CATACACGTT AGGGTCAGTT AAGGATGTTT GCTTTGGGTG 120 ATAGCCTACT TTTGGTCTCT TATTTATTAT CTGAGTACTA AGGTTTATCA ACTGAGTGTT 180 TTCTTCCCTT TCCTGGAAAA GGCAATGGAT GCAAGTGCCC TGATTTCTGA AATCTGAACC 240 TAGCCGGTAC AACATCAGGG CTGTGTCATG AGTCAGTGGC TTTGAAGCTG TCACACTGTC 300 ATTTTGCCTA ACTGCGGCTT TGAAGATTAG CCAGAGAGCC CTTTGAAGAA ACTTTCCTTT 360 AGTGTTGTGA ATAATACTTG AAAAGCCCAC AGCACTTGGT TTAATGTTGC AGTTGCAAAA 420 ACACTGACAG TTCCTATCCC ATAGAGCTGT TGAGTCATGT GGTTGAAGAC AGTTTTGGGG 480 AACCCGGTGC ACGTTCTGAA CCTGTAATGG GCTATGTTTG CTTACCAGGG CTAGCTCTCG 540 CTGACTTGGT CGTGTGCCTG GATGTAGGCA TTTTGTTTGC ACCCTTTCTG GATCGTGCCA 600 GGTTGTACAT AGCCCCAAGT GCCCCAGAGA AGCCAGGGAG GACAGAAGCG AAGGGCAGGG 660 GGGTGTCACC AGCATGCCGT TGGGACAGTC AGATGCGGAG GCGGCAGGAC CTTTTGGACC 720 ACAGTGCCCC GGCCGGACTC CTCAGGTGCT TGTGACGTGG GTGTGGACAT GTCCTGAGGC 780 AGGGCACCCT GGGCACCACG TTTCTGGCTG GCGACTTAGA CTCAAGCAGA TTAACCCCAT 840 GAAAGACGCC GATGAGGGCT GTCGTCCCCA AGTCTCCTGA AAAGTGGAGG TCAAGCAAGT 900 TTGAGCTGGT TATAGCCAAG CCCAGGCTGG ACTGGATCAT GTCTGAATCA GGAGTTGACT 960 GCTAGGCCTC AGGGGTGTCT GAGTTGTGCC ACCAGGGCGG CTCCTGAAGA CTCAGCTCAG 1020 GGTGAGGTCC TGGGGCTGCT GCGCACAGCC TGTCACCAGG TGGGGAAAGC TGCCCTGCAG 1080 TAACTGGGCT GGGGGGCCAG ATCCTCTAGA GATAGGGGTG CTTGGCTGGG TGCGGTGGCT 1140 GACACCTGTA ATCCCAGCAC TTTGGGAGGC CAAGGCAGGC AGATCACTTG AGGTCAGGAG 1200 TTCGAGACCA GCCTGGCCAA CATGGTGAAA CCCTGTCTCT ACTAAAAATA CAGAAATTAG 1260 CCGGGCGTGG TGGCAGACGC CTATAATCCC AGCTACTCAG GAGGCTGAGG CAGGAGAGTC 1320 GCTTGAACCT GGGAGAAGGA GGTTGCAGTG AGCCTAGATC GCGCCACTGC ACTCCAGCCT 1380 GGACAACAAG AGCAAGACTC TGTCTTTGGA AGAAAAAAAA ATTTTTTTAA AAAGGGAGGT 1440 GCTGCCCAAG AGGGAGGGGT CAGTACCTAA CTTGGGATGA AAGCCTAAGC TGCATGTCAG 1500 ACCAGCCTGG GAAGAGGCAG GCTGGACACA CTGCTGCCGG CTGGGAATGC CTCCGAAGTC 1560 AGAGTTGGAT GCTTTGAACA AGACCCCTCT AGCCTAATGT TGCTCATGAG CCTTTGGCGT 1620 TTTCATTCCA CGCAAGGTGG GCCCCTCTGA GCCAGCCAGC CTCCTTCCTT GTGCTGGTCA 1680 GACTTCAGAC CATTTCCTTC TGTTGATCAG CAAGTCCATG CCATTCCAGC ACATGGGAGC 1740 TTCACGGGAA GGAGACTGCT GTCCTCTGAA ACTGTACTGT GCGGTGCTGG CAGGTGCTTC 1800 GGAGCAGCTG AGCCTGCGTC TCCGAAGCTG GGAAAGGCAG AACAGGAGCT GCCCGTGCCT 1860 GCCCTGTTCT CAGCAGCAGT GGGCCTGCCT GCTCTCTCCA CATGGCGGCC TCCGCTGTAG 1920 ACACAGAAGA CAGATTTGCT CATTTTCTTT GGCTGCTGCT GTCTCCTCTC AGCCTTCTGC 1980 AAGGACCGTG GCCCATGTGA ACAGCCTTCC CTGAACCCTC CCGACACTCA TGCCTGCTTC 2040 AGACAACCTG GGGTGGGCTG CGGGCGTGAG AGGCTTTGGC CTGGCTGTGT CCCACAGGGG 2100 GCCTGTGTTG TGGATGGAGG ATGAGGTGTG GAAAAGGGAA TGAGGAAGAA AAAATGCAGG 2160 GATATTTTAA AGCCTTTTTA TTATCAAATA AGATACAGAT AAAAGTGCAA AACTAGACTG 2220 GGCATGGTGG CCCACACCTG TAATACTTTG GGAGGCTGAG GTGGGAGGAT TGCTTGAGGC 2280 CAGGAGCTCA AGACCAGCCT GAGCAACACA GTAAGACCAT GTCTCTACAA TAAATTTTAA 2340 AATTAGGTGG GTGGCACACA CCTGTAGTCA TAGCTACTTG GTAGGCTGAG GCAGGAGGAT 2400
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