Tag | Content |
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EnhancerAtlas ID | HS091-12343 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr14:20895280-20896960 |
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) |
NKX2-5 | MA0063.2 | chr14:20896137-20896147 | ACCACTTGAG | + | 6.02 | SPIC | MA0687.1 | chr14:20895990-20896004 | AGAAAGAGGAAGCA | + | 6.04 | ZNF263 | MA0528.1 | chr14:20895933-20895954 | GGAGAAAGAAGAGAAAGAAAA | + | 6.03 | ZNF263 | MA0528.1 | chr14:20895930-20895951 | GAGGGAGAAAGAAGAGAAAGA | + | 6.42 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28028 | chr14:20895260-20896705 | Fetal_Intestine | SE_29051 | chr14:20895241-20896718 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr14 | 20895335 | 20896697 | chr14 | 20895383 | 20896384 | chr14 | 20896422 | 20896678 | chr14 | 20895931 | 20896136 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I020426 | chr14 | 20894921 | 20897612 |
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Enhancer Sequence | ATGTATACAT ATGTAACTAA CCTGCACATT GGGCACATGT ACCCTAAAAC TTAAAGTATA 60 ATAATAATAA AATAAAATAA ATTAAAAAAA AAAAAAGAAA AAGAAAATTG ACCTAAACAC 120 ACACAAAAAA ACTGACCCTT TTTTGCTCTC AGCTGTCCAG TAGGCAGAAA TGGAAAGAGC 180 AGACAGGAAG GATAGAGGTG AGTCATAGAG GGCGGGAATA CACAATCATT AAGTGAAAGC 240 CATTATCCTC AGGAAGGCTC CAGAGAAGAG AGTAGGTGGC AAGAGCAGCA GAATTATCTG 300 AAAAGCCTCT GGAATACCCA CTTCCTCTTT GCTATGGAGA AACAGGGCAT GGCATGCCCC 360 ACTTCTTTCT GTTTCAAATG CATTCCCCCT TCTCTAATGG GTGAGACTCT AGGCAGCCTT 420 TAAGATCCAG TTCAAAATAC ACCCATCGGA TGACACCTTT CCTAACAGAA GCCTTCCTGA 480 GCAGAGTTCA CTGCTCTATC CTCTGGGCTC TCGCAAGACT CGTCCATACA TGTAAGTCCA 540 CTCAAAATTT GTATTTGTTT ATGTCTATCT GCTGGTCAGG AGCTCTCTGA CCTCTGTATC 600 TTGGTGCCTC CTACAGTGCC TGCCACACAG TAGGTAATTA ATAACTGTGT GAGGGAGAAA 660 GAAGAGAAAG AAAAAAGAGA GGCAGTGGGG AGAGCAGGAT GGGGGAAGAG AGAAAGAGGA 720 AGCACCTGAC TACCTTCCCT GGCCAAGATA AAGGGAAATG GATTTAAAAA TAACTCTGGG 780 GGAAAGGAAC TGAAAGGGGG AAATGACTTT TCTGAGTCTT GTCTGCTTCT CACTCTTCTC 840 TCCCCCCACA TCCTCTCACC ACTTGAGACC TCAGGCAACA ACGGTCTCAT TTTCACTCCT 900 GATTCCTCAG TTTGCCCAAA AGAAAGAAGG CACACAGGCT TCTGACTTCT TCCACCCCAT 960 CTCCTTAAAC CTCAGATCAT CTGTTTTTCC ACTGTGGGCC TCTCCCTCCT TGGCCTCTGC 1020 CCCCATCATC TTTCCCACAC AACACTCCTG CCACATGGCC CTGGGGGGCC CGTCAGGCCT 1080 CTCAGGCCCC TGTGCCGTGC ATGTCCATGT GGGAGCTTCT GCCTCAGAAG GAAACCAAGA 1140 GGTTCTCAGG GGCAGCCTGT GGTGTCTCGC TGGGAAACGC TAGACCAGGC CTACAAAGTT 1200 ACCCGGGAGA GAATATTGTT AAGAAGGTTT AGGCATCCCA GGGGTGGGAG AGGAGAAAGG 1260 AGCAAGTTCC AGGAAAAAAA GGGCTGAACG ATTTACAGTC CTTACTCCTA CACTCCTCAA 1320 ACTCTTTCAT GGATGGCCAT TCCACATTTT TCCCATGATC CATGGGTCAG AACCATTTTT 1380 CCAACTGTCC TCCCATGGTC TCTACACTTT GGCTACTGAA GCTTCTTAAC TCTCTTTCAA 1440 ACTAGATGCC CTTTCCCTAA GAATCCCTAA GCCTTGTGGA GTTGCTCCCG AGTCTCCTTT 1500 CCTCACCTGG GTATTCAGCT GCCTCCCCTT TCCCTATATG TTTTCCCTAG GAGTTCTGGA 1560 ACCACCATTT CCTCAACGGA GATCATACGT ACAAAAGCAG TTTACAATGC ACAGTGTGAG 1620 AATAAAATAC TACCAAGAAT AAAGCCTCTT TTCACTCCCC ACAATCTCTG TCCTTCTCTC 1680
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